Michigan Medicine, based in Ann Arbor, Michigan, is part of one of the world’s leading universities.

Michigan Medicine is a premier, highly ranked academic medical center and award-winning health care system with state-of-the-art facilities. Our vision is to create the future of health care through scientific discovery, innovations in education, and the most effective and compassionate care. 

We want to be the leader in health care, health care reform, and biomedical innovation.

Michigan Medicine includes the U-M Hospitals and Health Centers; the U-M Medical School and its Faculty Group Practice; one of the nation's largest biomedical research communities; and education programs that train thousands of future health professionals and scientists each year. We were formerly known as the University of Michigan Medical Center; today that term applies generally to the collection of buildings on our main medical campus in Ann Arbor. 

We have a close partnership with the U-M School of Nursing and other health sciences schools at U-M. Through  the Michigan Health Corporation, we are able to form partnerships outside of our University.

Industry: Hospitals and Health Care
Company Size: 10,001+ employees

Michigan Medicine

Savvy Admin PROD

How to Apply

A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

**Job Summary**

The Department of Cell & Developmental Biology is seeking a full-time Research Laboratory Technician Associate in the lab of Dr. Cai, which studies neuronal circuitry and neurogenesis in mouse and fly brains.

Responsibilities*

We are seeking a motivated and detail-oriented Laboratory Technician Associate to support ongoing research in a collaborative neuroscience laboratory. The successful candidate will contribute to experimental workflows, data analysis, and general laboratory operations.

Primary responsibilities include performing routine molecular and cellular biology techniques such as molecular cloning, immunohistochemistry, fluorescence microscopy, and quantitative image analysis.

Additional responsibilities include preparing stock solutions and reagents, maintaining laboratory supplies and equipment, sterilizing glassware, and ensuring a clean and organized laboratory environment. The technician will also assist with general laboratory management tasks and may support other research activities as needed.

Required Qualifications*

Excellent written and verbal communication skills, as well as interpersonal skills contributing to a strong team environment are required.

Bachelors in biology or related science degree and at least 1 years' experience.

Applicant should be highly motivated with thorough, methodological, and accurate work habits, and must be able to work as part of a team.

The ideal candidate has a strong ability to multi-task.

Desired Qualifications*

- Previous lab research experience.

Why Join Michigan Medicine?

Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.

**What Benefits can you Look Forward to?**

- Excellent medical, dental and vision coverage effective on your very first day

- 2:1 Match on retirement savings

Modes of Work

Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.

Background Screening

Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.

Application Deadline

Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.

U-M EEO Statement

The University of Michigan is an equal employment opportunity employer.

Research Laboratory Tech Assoc

The mission of the University of Michigan is to serve the people of Michigan and the world through preeminence in creating, communicating, preserving, and applying knowledge, art, and academic values, and in developing leaders and citizens who will challenge the present and enrich the future.

Why Work at Michigan?

Being part of something greater, of serving a larger mission of discovery and care — that's the heart of what drives people to work at Michigan. In some way, great or small, every person here helps to advance this world-class institution. It's adding a purpose to your profession. Work at Michigan and become a victor for the greater good.

Industry: Higher Education
Company Size: 10,001+ employees

University of Michigan

Welcome to DataAnnotation! We pay smart folks to train AI. We offer a remote, flexible work model- you choose your own hours and get to work when you want, whenever you want. Apply now through our open Job Listings.

Industry: Software Development
Company Size: 5,001-10,000 employees

DataAnnotation

We are looking for a Research Scientist (Chemistry) to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.

In this role you will need to hold an expert level understanding of chemistry. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.

**Benefits**

- This is a full-time or part-time REMOTE position

- You’ll be able to choose which projects you want to work on

- You can work on your own schedule

- Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots complex chemistry questions and evaluate their outputs

- Evaluate the quality produced by AI models for correctness and performance

**Qualifications**

- Fluency in English (native or bilingual level)

- Detail-oriented

- Solid knowledge of general, organic, and physical chemistry concepts

- A current, in progress, or completed Masters and/or PhD is preferred but not required

**Notes**

Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Only applicants in the United States will be considered for this role. This is an independent contract position.

#chem

Research Scientist (Chemistry)

Bell International Laboratories, Inc, is located in Eagan, Minnesota.  We specialize in Health, Beauty and Cosmetic Manufacturing.  Our expertise is in Sun Care, Skin Care, Hair Care,  OTC and Nutritional products.  We offer R&D services as well as product manufacturing.  Bell International Laboratories is fully certified and regulated by the FDA, and is ATF,EPA and Minnesota Department of Health registered.

Industry: Personal Care Product Manufacturing
Company Size: 201-500 employees

Bell International Laboratories

The Analytical Laboratory Chemist is pivotal in conducting and managing analytical testing of raw materials, in-process samples, and finished products to ensure compliance with cGMP standards. This role supports the Quality Control Lab Manager in upholding the integrity and quality of the laboratory environment.

**Responsibilities: **

- Develop and validate analytical methods to ensure reliability and accuracy of test results.

- Operate and maintain sophisticated laboratory instruments, including HPLC, GC, UV-Vis, and FTIR.

- Conduct routine calibration and validation of laboratory instruments to maintain compliance with operational standards.

- Prepare and analyze samples from raw materials, in-process batches, and finished products using both wet chemistry techniques and instrumental analysis.

- Maintain meticulous laboratory records and notebooks, ensuring detailed documentation following regulatory requirements.

- Collaborate with team members to efficiently complete testing assignments within set timelines.

- Monitor ongoing product quality to confirm adherence to established standards and specifications.

- Adhere to Standard Operating Procedures (SOPs) and global methodological standards such as USP, AOCS, and ASTM.

- Troubleshoot and perform minor repairs on analytical instruments to minimize downtime.

- Implement safety protocols for handling chemicals, managing laboratory waste, and maintaining a clean lab environment.

- Organize and manage laboratory inventory to ensure availability of necessary supplies and equipment.

- Mentor and train new laboratory personnel on testing procedures and instrument operations.

**Required Skills/Abilities: **

- Proficient in the use of standard laboratory equipment and familiar with advanced analytical techniques.

- Excellent communication skills, both verbal and written, with the ability to convey complex information clearly.

- Strong analytical thinking and problem-solving capabilities.

- Effective time management skills to handle multiple tasks and meet strict deadlines.

- Demonstrated ability to work autonomously in a dynamic, fast-paced environment.

- Keen attention to detail with a commitment to high-quality work.

- Flexibility to adapt to new procedures or rapid changes in project priorities.

- Proficient in Microsoft Office

**Required Education and Experience: **

- Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.

- 3 to 5 years of hands-on experience in an analytical laboratory setting, preferably within the personal care, pharmaceutical, or related industries.

- Extensive knowledge of cGMP practices, organic chemistry, and instrumental analytics (HPLC, GC, UV-Vis, FTIR).

Analytical Chemist

Astrix is the unrivaled market-leader in creating & delivering innovative strategies, solutions, and people to the life science community.  

Through world class people, process, and technology, Astrix works with clients to fundamentally improve business & scientific outcomes across many domains including the laboratory, clinical & regulatory, pharmacovigilance, R&D, and manufacturing. 

Founded by scientists to solve the unique challenges of the life science community, Astrix offers a growing array of strategic, application & platform, data transformation & analytics, change management, and staffing services designed to deliver immediate value to clients and solve their most complex technical and staffing challenges.

Industry: IT Services and IT Consulting
Company Size: 1,001-5,000 employees

Astrix

Pay Rate Low: 40 | Pay Rate High: 45

Seeking a Chemist to join a world leader in science. Opportunity to join an R&D Analytical Characterization team, supporting chromatography and wet chemistry testing of materials used in medical/surgical products. This role focuses on analyzing small organic compounds, additives, degradation products, and impurities in complex polymer systems.

Key Responsibilities

- Perform analytical testing using GC, Headspace GC, and U/HPLC-UV.

- Conduct full workflows including sample preparation, method execution/qualification, data analysis, and reporting.

- Investigate and report issues such as OOS/OOT results, instrument problems, and lab deviations.

- Troubleshoot and maintain analytical instruments.

- Document work in compliance with FDA/ICH standards and internal procedures.

- Communicate results clearly through written reports and presentations.

- Support preparation of technical reports and documentation

**Qualifications**

- BS, MS, or PhD in Chemistry (Analytical, Polymer, Organic) or related field

- ~1–2+ years of relevant experience (depending on degree level)

- Familiarity with medical device or regulated environments preferred

- Strong foundation in analytical chemistry principles

- Hands-on experience with GC and HPLC instrumentation

- Experience with method development/validation (preferred)

Pharmaron: Global Life Sciences Services Provider
Stock Code: 300759.SZ/3759.HK

Founded in 2004, Pharmaron is a premier life sciences service provider that offers a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. 

Pharmaron’s Comprehensive CRO & CDMO Services 
•	Synthetic, Medicinal, and Analytical Chemistry Services
•	Biology Services (e.g., in vitro screening, structural biology, biomarkers)
•	DMPK Services (e.g., in vitro ADME, in vivo PK, PKPD, mass balance)
•	Pharmacology Services (e.g., in vivo pharmacology, animal disease models, immunotoxicity)
•	Drug Safety Assessment Services (e.g., toxicology, safety pharmacology, genetic toxicology)
•	Radiochemistry and Isotopically Labelled Metabolism Services (e.g., 14C/Carbon-14 radiosynthesis, 3H/tritium radiosynthesis, QWBA, mARG)
•	CMC Services (e.g., API manufacturing, process chemistry, formulation development)
•	Clinical Development Services (e.g., First-in-Human [FIH], ethnobridging, microdosing Phase 0, absolute bioavailability)

Commitment to Excellence and Innovation

With a proven track record of success, Pharmaron continually invests in its people, facilities, and technologies to meet evolving scientific and regulatory demands. The company prides itself on enabling scientific breakthroughs and supporting its partners in advancing human health.
_

Learn More:  Explore Pharmaron’s services to discover how to accelerate your R&D programs. www.pharmaron.com.

_

Keywords:  CRO, CDMO, synthetic chemistry, medicinal chemistry, biology, radiochemistry, toxicology, First-in-Human, API manufacturing, PKPD, 14C radiosynthesis, discovery biologics, clinical development, small molecules, biologics, cell and gene therapy (CGT) products

Industry: 制药业
Company Size: 超过 10,001 人

Pharmaron

**Position **: Senior Scientist – Analytical Chemistry

**Salary Range: **$90k - $130k

**Location: **Coventry, RI

**About Pharmaron**

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We're proud of the impact we make and just last year, we supported over **780 discovery projects **, **1,000+ CMC programmes **, and **1,000+ clinical trials **across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than **3,000 global customers **. To learn more, visit www.pharmaron.com.

**Job Overview**

The Senior Scientist - Analytical Chemistry will serve as a key technical resource within the Quality Control laboratory supporting API manufacturing and development programs at Pharmaron's Coventry, RI facility.

This role is responsible for supporting analytical method validation, transfer, troubleshooting, and QC testing of raw materials, intermediates, and active pharmaceutical ingredients in a cGMP-regulated laboratory environment. The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations.

**Key Responsibilities**

- Support analytical method validation, verification, and transfer activities within the QC laboratory.

- Troubleshoot complex analytical challenges related to API characterization and GMP testing.

- Review analytical data, laboratory notebooks, and instrument qualification documentation to ensure scientific accuracy and regulatory compliance.

- Lead or support laboratory investigations, deviations, and root cause analyses.

- Maintain laboratory equipment and serve as system owner for analytical instrumentation, including qualification and maintenance activities.

- Provide technical mentorship and scientific guidance to QC scientists and laboratory personnel.

- Prepare and revise standard operating procedures (SOPs), analytical methods, and technical documentation.

- Support internal and external regulatory inspections and client audits as an analytical subject matter expert.

- Collaborate with cross-functional teams including Manufacturing, Process Chemistry, Quality Assurance, and Regulatory Affairs.

- Contribute to continuous improvement initiatives that enhance QC laboratory efficiency and analytical capabilities.

- Perform other related assignments and duties, as required and assigned.

**What We're Looking For**

- Ph.D. in Chemistry or a related field with 1–4 years of postdoctoral or industry experience.

- MS with 5–8 years of pharmaceutical industry experience, BS with 7–10 years of relevant pharmaceutical industry experience

- 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, UV, Mass Spectrometry.

- Demonstrated experience applying analytical techniques to solve complex scientific problems related to method validation, troubleshooting, and implementation

- Strong hands-on expertise with analytical instrumentation including:

- HPLC / UPLC

- GC

- FTIR

- UV

- Mass Spectrometry

- Experience supporting API manufacturing or pharmaceutical QC laboratories

- Proven ability to troubleshoot analytical instrumentation and laboratory methods

- Working knowledge of cGLP / cGMP and applicable FDA, EMA, and ICH regulatory guidelines

- Experience contributing to multidisciplinary scientific teams and cross-functional projects

- Experience mentoring or supervising laboratory personnel preferred

- Strong analytical thinking, scientific judgment, and problem-solving skills

- Excellent written and verbal communication skills

**Why Pharmaron?**

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

**Collaborative Culture: ** You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

**Benefits:**

As part of our commitment to your well-being, we offer a comprehensive benefits package:

- Insurance including Medical, Dental & Vision with significant employer contributions

- Employer-funded Health Reimbursement Account

- Healthcare & Dependent Care Flexible Spending Accounts

- 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance

- 401k plan with generous employer match

- Access to an Employee Assistance Program

**How to Apply:**

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

**About Pharmaron**

Pharmaron (Stock Code: 300759.SZ/3759.HK) is a premier R&D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products. With over 19,000 employees, and operations in China, the U.S., and the U.K., Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China.

Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer.

Senior Scientist – Analytical Chemistry

Belcan, a Cognizant company is a global supplier of engineering, manufacturing & supply chain, workforce and government IT solutions to customers in the aerospace, defense, commercial vehicles & automotive, industrial, and private sector. We engineer better outcomes for our customers – from jet engines, airframe, and avionics to heavy vehicles, automobiles, and cybersecurity. 

Taking a partnering approach to provide solutions that are adaptable, integrated, and value added, we have been earning the trust of our customers for over 60 years and counting.

Industry: Information Technology & Services
Company Size: 5,001-10,000 employees

Belcan

Job Title: Research Associate I

Location: Wilmington, DE

Zip Code: 19803

Pay Rate: $30-33/hr

Keyword's: #Wilmingtonjobs; #Associatejobs.

Start Date: Immediate

Job Description:

Responsibilities:* Lead application focused research efforts that provide direct technical support to R&D projects in paints and coatings, construction materials, water, and the energy industries, fostering innovation.

* Contribute to the development of novel formulations using new and existing active ingredients and next-generation delivery technologies.

* Utilize analytical chemistry techniques, including HPLC, to characterize the performance criteria of new formulations.

* Collaborate with lead scientists, other research associates, and broader interdisciplinary teams, including regulatory, marketing, and product development, to support and drive projects from concept to commercialization.

* Effectively manage time across multiple projects and competing demands, demonstrating a proactive approach to execution.

* Maintain a safe and organized laboratory environment while assuring compliance with safety regulations.

Qualifications:* Bachelors or Masters degree in Chemistry, Biochemistry, or Chemical Engineering.

* A minimum of 3 years of industrial laboratory experience in a research, product development, or technical application setting.

* Prior experience with analytical techniques (HPLC) and industrial product formulation a plus.

* Strong written and verbal communication skills, with the ability to collaborate across teams.

* Self-motivated with the ability to manage multiple projects and shifting priorities in a fast-paced environment.

* Strong problem-solving skills and creative thinking.

* Experience working in a team-oriented research setting to drive projects toward completion preferred.

Associate Researcher

ARL Bio Pharma is a contract laboratory that provides analytical and microbiological testing for the pharmaceutical industry. Since 1998, ARL has supported the industry-wide commitment to deliver high-quality drug products by providing guidance and test services for all phases of the product lifecycle following USP, FDA, and ICH guidelines.

Whether you are a raw material supplier, equipment manufacturer, pharmaceutical manufacturer, pharmacy, or health-system we provide the testing needed to get your drug products ready for release.

ARL’s dedicated team oversees the entire process from understanding your goals to providing results and helping interpret the data.

ARL Bio Pharma is an FDA registered and audited analytical laboratory and DEA licensed for Schedules I through V. The laboratory is ISO 17025:2017 accredited as applicable to our scope of accreditation. 17025:2017 accreditation independently demonstrates ARL's ability to not only comply with quality requirements, but to competently perform specified tests and activities.

Industry: Pharmaceutical Manufacturing
Company Size: 201-500 employees

ARL Bio Pharma

Chemist I - Analytical

Position Summary

Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer.  This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry.  The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations.

**Some highlights... **

- Paid Training

- Work in a comfortable office setting with casual dress code

- Have your own workspace where you can work largely independently

- Free Medical and Dental insurance

- 401K Retirement with Company Match

- Excellent Work/Life Balance

This is a full-time role with a great benefits package.

**Work Schedule: ** 7:00 am - 4:30pm

**Restrictions: **  Because of vital nature of this work, we do not allow medical marijuana cards and we do random drug testing on all of our employees.

**Essential Functions **

- Adhere to Quality Management System (QMS)

- Follow prescribed safety rules and regulations in performing all assigned duties

- Follow written and oral instruction

- Prepare reagents and solutions required for testing

- Perform laboratory testing and record results in compliance with cGMP’s (if applicable) and internal QMS

- Work and think independently, yet share ideas and work towards team goals

- Use a personal computer including word processing, spreadsheets, email and database applications

- Express thoughts in a clear concise manner both orally and written

- Work to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities

- Adherence to all ARL safety standards, protocols, policies and procedures

**Position Requirements... **

- An associate degree in chemistry or related science with 2+ years industrial experience OR...

- Bachelor’s degree in chemistry or related science with 1-2 years’ experience in the Pharmaceutical industry.

- Communication Proficiency

- Problem Solving/Analysis

- Organization/Multi-tasking

- Collaboration Skills

- Thoroughness

**Work Environment... **

This job operates in a laboratory environment.

**Physical Demands... **

The role requires standing for prolonged periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stoop; ability to lift and move up to 50 pounds; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction.

AAP/EEO Statement

ARL Bio Pharma, Inc.  provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law.  ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law.  Improper interference with the ability of ARL Bio Pharma, Inc.  employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics.

About Genentech

We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal.

Making a difference in the lives of millions starts when you make a change in yours. If you’d like to join our team, view our openings at gene.com/careers. 

Our patient resource center is dedicated to getting patients and caregivers to the right resources. You can reach them at 1 (877) GENENTECH (436-3683)
Monday-Friday, 6am-5pm PST or patientinfo@gene.com. 

Community Guidelines:

1. We want to foster positive conversation around the issues we are passionate about. To that end, we remove profanity, content that contains threatening language, content that is aimed at private individuals, personal information, and repeated unwanted messages.

2. Don’t mention any medicines by name — ours or anyone else’s.
Because of the fair balance rules governing our industry, we cannot post any comments that reference any pharmaceutical brand, product, or service. Please do not mention any specific medicines by name, or include any links to third party sites in your comments.

3. This isn’t the place to report or discuss side effects.
This site is not intended as a forum for reporting side effects experienced while taking a Genentech product. Instead, you should report any side effects to Genentech Drug Safety at 1-888-835-2555. You can also report side effects of any prescription product directly to the FDA at 1-800-FDA-1088 or by visiting www.FDA.gov/medwatch.

4. Don’t pitch your product or service.
Please don't use our page as a place to promote your product or pitch your services. Please also avoid posting links to external sites. We reserve the right to remove any posts that are deemed promotional.

Industry: Biotechnology Research
Company Size: 10,001+ employees

Genentech

The Position

We advance science so that we all have more time with the people we love.

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Genentech!

**The Opportunity:**

We are seeking a highly motivated Senior Scientist or Principal Scientist with a strong record of laboratory innovation and technical depth to join our Synthetic Molecule Analytical Chemistry (SMAC) group.

This role is ideal for a scientist who thrives at the bench and is excited to solve complex analytical challenges, while contributing to advancing programs spanning discovery through clinical development.

The Scientist will play a key role in advancing a diverse pipeline including synthetic small molecules, peptides, oligonucleotides, and drug delivery systems (e.g., lipid nanoparticles, polymer nanoparticles), working in a highly collaborative, cross-functional environment:

- Designing, developing, and troubleshooting analytical methods from first principles, including sample preparation, method optimization, and data interpretation with state-of-the-art technologies including but not limited to high resolution mass spectrometry (HRMS), UHPLC, 2D-LC/MS, GC/MS, light scattering, spectroscopy, rheology, microscopy.

- Applying and deepen expertise in HRMS, MS/MS, and/or chromatographic separations to solve complex analytical problems during drug discovery/development.

- Contributing to regulatory submissions, including authoring sections and preparing data packages for health authority interactions.

- Partnering with cross-functional teams (process development, formulation, safety science, quality, etc.) to develop control strategies aligned with cGMP, ICH, and regulatory expectations.

- Informing program decisions across discovery and early development, i.e. generating high-quality data to guide molecular and formulation decisions

- Innovating and evaluating new technologies in analytical chemistry or materials characterization to enable the integration of state-of-the-art instrumentation and software to solve complex problems.

- Maintaining a high-level scientific profile both internally and externally in terms of pipeline contributions and scholarly achievements.

**Who You Are**

Successful candidates will possess the following qualifications:

- PhD in Analytical Chemistry, Pharmaceutical Sciences, Materials Sciences, Bioengineering, or relevant scientific disciplines with

0-2 years industry experience ( Senior Scientist); 3-5 years of industry experience (Principal Scientist). Exceptional candidates with Bachelor or Master degree in these fields with 12+ years of experience may be considered. Title and level will be aligned with qualifications and experience.

- Outstanding record of innovation and success in multiple projects over the course of graduate, post-doctoral and industrial career with a sustained publication or patent record.

- Deep hands-on expertise in at least one of the following areas for the analysis of synthetic small molecules, peptides, oligonucleotides, polymers, or nanoparticles (lipid and polymer nanoparticles) is required:

- Mass spectrometry method development (HRMS, MS/MS, structural elucidation)

- Chromatographic method development (reversed phase, normal phase, HILIC, SEC, SFC, 2D-LC/MS)

- Experience with chromatography and/or MS data systems (e.g., Empower, Xcalibur, MassHunter, Chromeleon), and ability to independently analyze complex datasets, is required.

- Experience with nanoparticle-based drug delivery systems (lipid nanoparticles, polymer nanoparticles, etc.) is highly desirable.

- Excellent communication (orally and in writing) and organizational skills.

- Ability to collaborate, learn, and eventually lead in a CMC/cross functional environment.

- Ability to take initiative, think strategically, work in teams and develop people, have advanced literature searching and problem-solving skills.

**Preferred:**

- Knowledge of the chemistry and formulation processes of nanoparticle-based drug delivery systems (e.g., lipid nanoparticles, polymeric systems).

- Exposure to CMC, regulatory submissions, or analytical control strategies.

- Working knowledge of data analysis, modeling, and AI assisted workflows, including the ability to effectively use AI tools (e.g., LLM).

- Familiarity with additional characterization tools (e.g., light scattering, rheology, spectroscopy, microscopy).

Relocation benefits are available for this posting.

The expected salary range for this position based on the primary location of California for Senior Scientist is $124,300- $230,900 and Principal Scientist is $143,200-$265,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

**Benefits**

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Senior/ Principal Scientist, Synthetic Molecule Analytical Chemistry

The Position

We advance science so that we all have more time with the people we love.

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Genentech!

**The Opportunity:**

We are seeking a highly motivated Senior Scientist or Principal Scientist with a strong record of laboratory innovation and technical depth to join our Synthetic Molecule Analytical Chemistry (SMAC) group.

This role is ideal for a scientist who thrives at the bench and is excited to solve complex analytical challenges, while contributing to advancing programs spanning discovery through clinical development.

The Scientist will play a key role in advancing a diverse pipeline including synthetic small molecules, peptides, oligonucleotides, and drug delivery systems (e.g., lipid nanoparticles, polymer nanoparticles), working in a highly collaborative, cross-functional environment:

- Designing, developing, and troubleshooting analytical methods from first principles, including sample preparation, method optimization, and data interpretation with state-of-the-art technologies including but not limited to high resolution mass spectrometry (HRMS), UHPLC, 2D-LC/MS, GC/MS, light scattering, spectroscopy, rheology, microscopy.

- Applying and deepen expertise in HRMS, MS/MS, and/or chromatographic separations to solve complex analytical problems during drug discovery/development.

- Contributing to regulatory submissions, including authoring sections and preparing data packages for health authority interactions.

- Partnering with cross-functional teams (process development, formulation, safety science, quality, etc.) to develop control strategies aligned with cGMP, ICH, and regulatory expectations.

- Informing program decisions across discovery and early development, i.e. generating high-quality data to guide molecular and formulation decisions

- Innovating and evaluating new technologies in analytical chemistry or materials characterization to enable the integration of state-of-the-art instrumentation and software to solve complex problems.

- Maintaining a high-level scientific profile both internally and externally in terms of pipeline contributions and scholarly achievements.

**Who You Are:**

Successful candidates will possess the following qualifications:

- PhD in Analytical Chemistry, Pharmaceutical Sciences, Materials Sciences, Bioengineering, or relevant scientific disciplines with 0-2 years industry experience ( Senior Scientist); 3-5 years of industry experience (Principal Scientist). Exceptional candidates with Bachelor or Master degree in these fields with 12+ years of experience may be considered. Title and level will be aligned with qualifications and experience.

- Outstanding record of innovation and success in multiple projects over the course of graduate, post-doctoral and industrial career with a sustained publication or patent record.

- Deep hands-on expertise in at least one of the following areas for the analysis of synthetic small molecules, peptides, oligonucleotides, polymers, or nanoparticles (lipid and polymer nanoparticles) is required:

- Mass spectrometry method development (HRMS, MS/MS, structural elucidation)

- Chromatographic method development (reversed phase, normal phase, HILIC, SEC, SFC, 2D-LC/MS)

- Experience with chromatography and/or MS data systems (e.g., Empower, Xcalibur, MassHunter, Chromeleon), and ability to independently analyze complex datasets, is required.

- Excellent communication (orally and in writing) and organizational skills.

- Ability to collaborate, learn, and eventually lead in a CMC/cross functional environment.

- Ability to take initiative, think strategically, work in teams and develop people, have advanced literature searching and problem-solving skills.

**Preferred:**

- Exposure to CMC, regulatory submissions, or analytical control strategies.

- Working knowledge of data analysis, modeling, and AI assisted workflows, including the ability to effectively use AI tools (e.g., LLM).

Relocation benefits are available for this posting.

The expected salary range for this position based on the primary location of California for Senior Scientist is $124,300- $230,900 and Principal Scientist is $143,200-$265,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

**Benefits**

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Senior/Principal Scientist - Synthetic Molecule Analytical Chemistry, Genentech Research and Early Development

ADM unlocks the power of nature to enrich the quality of life. We’re a premier global human and animal nutrition company, delivering solutions today with an eye to the future. We’re blazing new trails in health and well-being as our scientists develop groundbreaking products to support healthier living. We’re a cutting-edge innovator leading the way to a new future of plant-based consumer and industrial solutions to replace petroleum-based products. We’re an unmatched agricultural supply chain manager and processor, providing food security by connecting local needs with global capabilities. And we’re a leader in sustainability, scaling across entire value chains to help decarbonize our industry and safeguard our planet. From the seed of the idea to the outcome of the solution, we give customers an edge in solving the nutritional and sustainability challenges of today and tomorrow. Learn more at www.adm.com.

Industry: Food and Beverage Manufacturing
Company Size: 10,001+ employees

Analytical Chemistry / Chemometrics Support

This position is located in the ADM R&D Analytical Laboratory, which provides analytical support across ADM’s global portfolio. This role may support both laboratory analyses and applied chemometric and statistical workflows, working closely with senior scientists and cross‑functional teams.

An ideal candidate will have strong hands‑on experience in analytical laboratory techniques, along with familiarity or applied exposure to chemometrics, statistics, or modeling concepts gained through academic coursework or professional experience. This position offers the opportunity to continue developing expertise across a variety of analytical and data analysis techniques through structured technical guidance and mentorship.

**Key Responsibilities**

- Ensure safe work practices are applied for all tasks in the laboratory and throughout ADM facilities.

- Perform routine and non‑routine analytical testing using advanced techniques such as LC/MS, HPLC, GC/MS, GC, ICP, ICP‑MS, FTIR, and laboratory robotics.

- Support the development, optimization, and implementation of analytical methods to meet the needs of ADM business units and customers.

- Assist with chemometric and statistical workflows associated with routine analytical methods and process monitoring, including data preparation, exploratory analysis, model execution, and basic performance evaluation.

- Generate high‑quality laboratory data to support model development, validation, maintenance, and monitoring.

- Contribute to R&D projects requiring analytical data and applied modeling support under the technical direction of senior scientists.

- Collaborate with chemists, engineers, data scientists, and operations partners on cross‑disciplinary projects.

- Communicate results, observations, and potential issues clearly to project stakeholders.

- Perform routine instrument maintenance and basic troubleshooting.

- Prioritize assigned tasks to meet project timelines in a dynamic environment.

- Continue professional development through training, mentoring, and hands‑on experience.

Job Requirements

**Required**

- Bachelor’s or Master’s degree in Chemistry, Biochemistry, Chemical Engineering, Statistics, Data Science, or a closely related field.

- 3–5 years of relevant hands‑on laboratory experience in analytical chemistry or spectroscopy.

- Strong practical experience with analytical laboratory techniques, including chromatographic and/or spectroscopic methods.

- Familiarity with chemometrics, statistics, or modeling concepts.

- Working knowledge of data analysis tools such as JMP, R, Python, Unscrambler, PLS Toolbox, or similar platforms.

- Ability to work independently on defined tasks while contributing effectively within a team environment.

- Strong written and verbal communication skills.

- Understanding of laboratory safety practices and the safe handling of hazardous materials.

**Preferred**

- Experience with food, feed, fermentation, or agricultural matrices.

- Interest in continued growth in chemometrics, spectroscopy, or advanced analytics.

Excited about this role but don’t think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings.

ADM requires the successful completion of a background check.

REF:107220BR

Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours.

If hired, employees will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

The pay range for this position is expected to be between:

$70,400.00 - $129,000.00

**Salaried Incentive Plan**

The total compensation package for this position will also include annual bonus

**Benefits And Perks**

Enriching the quality of life for the world begins by taking care of our colleagues. In addition to competitive pay, we support your diverse needs with a comprehensive total rewards package to enhance your well-being, including:

- Physical wellness – medical/Rx, dental, vision and on-site wellness center access or gym reimbursement (as applicable).

- Financial wellness – flexible spending accounts, health savings account, 401(k) with matching contributions and cash balance plan, discounted employee stock purchasing program, life insurance, disability, workers’ compensation, legal assistance, identity theft protection.

- Mental and social wellness – Employee Assistance Program (EAP), Employee Resource Groups (ERGs) and Colleague Giving Programs (ADM Cares).

**Additional Benefits Include**

- Paid time off including paid holidays.

- Adoption assistance and paid maternity and parental leave.

- Tuition assistance.

- Company-sponsored training and development resources, such as LinkedIn Learning, language training and mentoring programs.

*Benefits may vary for bargained locations, confirm benefit eligibility with your recruiter.

**#IncludingYou**

Diversity, equity, inclusion and belonging are cornerstones of ADM’s efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments — environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together.

We welcome everyone to apply. We are committed to ensuring all qualified applicants receive consideration for employment regardless of race, color, ethnicity, disability, religion, national origin, language, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law

**About ADM**

At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We’re a global leader in human and animal nutrition and the world’s premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at www.adm.com.

**Req/Job ID**

107220BR

Scientist III - Decatur, IL

Since the beginning, ZRT has maintained a singular focus: helping people get and stay healthy.

With 20 years of experience and results from over 8 million tests, ZRT Laboratory is a recognized leader in innovative and meaningful hormone, neurotransmitter and elements testing. 

Individuals, health care providers in all 50 states and 90 countries, and research teams worldwide use our tests, including the CDC, the NIH and many renowned universities.

ZRT is the recognized leader in saliva and dried blood spot testing for hormones, and holds the distinction of being the lab that developed dried urine testing for hormones.

ZRT was founded and is led by David Zava, PhD, a renown expert in hormones and breast cancer. He is an author, researcher and frequent lecturer at industry events.

Learn more about the role of hormones, neurotransmitters and elements in our health at https://www.zrtlab.com/blog/.

Industry: Hospitals and Health Care
Company Size: 51-200 employees

ZRT Laboratory

ZRT Laboratory is an internationally recognized leader in hormone and wellness testing. For over 27 years, healthcare providers and academic research teams worldwide have trusted our expertise in accurately measuring hormones, neurotransmitters, and elements in saliva, finger-stick dried blood, dried urine, and serum. With results from over 10 million tests, ZRT offers a commitment to the best science and the best people, delivering premier personalized home-collection testing solutions.

**Position Summary: **

As an Analytical Chemist at ZRT Laboratory, you will play a hands-on role in the development and execution of LCMS and GCMS methodologies, contributing directly to the accuracy and advancement of our hormone and wellness testing. Working in our CLIA-certified high complexity laboratory, you will analyze complex biological samples, support method development, and help ensure the quality and integrity of results that matter to patients and providers worldwide.

**Key Responsibilities: **

~~Production & Analysis: ~~

- Perform commercial, clinical, and research sample preparation, analysis, and documentation

- Create and maintain assay standards, calibrators, and controls

- Rotate between laboratory areas as needed

~~Instrumentation & Laboratory Operations: ~~

- Operate and maintain a wide range of instrumentation

- Prepare reagents, manage inventory, and perform equipment maintenance

- Handle biohazard waste disposal

~~Data Management & Documentation: ~~

- Ensure accuracy of data and maintain records

- Document and communicate ongoing and completed projects promptly

~~Quality & compliance: ~~

- Maintain competency in assigned testing procedure

- Ensure compliance with SOPs and state and federal regulations

- Maintain HIPAA compliance

- Adhere to proper hand hygiene and PPE protocols

~~Professional Development & Administrative Support: ~~

- Participate in continuing education programs

- Support ordering and budgeting activities

**Competencies: **

- Strong problem-solving skills to troubleshoot LCMS/GCMS issues and optimize methods

- Strong written and verbal communication skills for clear reporting and presentation of analytical results

- Detail-oriented with a strong commitment to maintaining high data quality and laboratory standards

- Ability to work both independently and collaboratively within a team

Required Education and Experience:

- Master's degree or higher in Analytical Chemistry or a related field

- Five years of prior LC/GC-MS experience including instrument operation and data analysis

ZRT Laboratory is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where all employees feel valued and supported.

Job Type: Full-time

Benefits:

- 401(k)

- 401(k) matching

- Dental insurance

- Employee assistance program

- Employee discount

- Flexible schedule

- Flexible spending account

- Health insurance

- Life insurance

- Paid time off

- Parental leave

- Referral program

- Tuition reimbursement

- Vision insurance

Analytical Chemist - LCMS

Wiley’s leading media brand providing first-hand information on the global chemical, life science and process industries

Industry: Zeitungsverlage
Company Size: 201–500 Beschäftigte

CHEManager International

**Job Title**

Scientist II, Analytical Chemistry

**Job Description**

**The Role:**

Our site in **Burnet, TX **is seeking a **Scientist II, Production Analytical Chemist, ** to join our team. Come help analyze and characterize the materials that help design, deliver, and optimize some of the most critical semiconductor devices in the world. Be a part of a team and organization that is pushing the boundaries of chemical manufacturing through your expertise as an analytical chemist!

We are seeking a Chemist with in-depth knowledge of analytical chemistry and techniques applied to the characterization of complex mixtures. This knowledge is required to troubleshoot, develop, and optimize analytical methods for routine and non-routine QC analysis to support the Manufacturing and Engineering Teams. Due to the complex nature of sample matrices, this opportunity allows the right person to expand upon their technical skill set and participate on a dynamic team in a growing organization.

The ideal candidate will be results and detail oriented, strive to be an excellent team player, and be able to apply their solid knowledge of chemistry, mechanical inclination, good lab practices, and familiarity with the criticality of materials science in the semiconductor industry.

**What You'll Do**

- Demonstrate leadership in maintaining safety and quality culture

- Prepare and conduct chemical and/or physical analyses as defined by existing work instructions on routine and non-routine samples using analytical instruments including: ICP-MS, ICP-OES, GC, GC/MS, HPLC, IC, XRF, UV-Vis, NIR, KF, etc.

- Document, process, transfer, and review analytical data to ensure completion, conformity, traceability, and validity and support production and other internal/external customer needs; Take corrective action when necessary

- Maintain instrumentation, tools, chemicals, and consumables required for product testing purposes

- Effectively troubleshoot instruments and resolve any hardware or software issues

- Verify the efficacy of samples and ensure that all samples and chemicals are properly stored or disposed

- Propose/Lead/Support initiatives to foster continuous improvement of new or existing testing methods and practices

- Maintain housekeeping and proper Laboratory cleanliness to support high quality trace-level data

- Compile and present data and presentations to communicate data and other relevant information for continuous improvement, method development/validation, and other projects

- Work on cross-functional teams as the analytical subject matter expert

- Train other personnel to analyze samples or perform other laboratory tasks

**What We Seek**

- A minimum of a Bachelor's Degree in Analytical Chemistry or relevant area of study is required.

- 2+ years of experience in operating, troubleshooting, and maintaining analytical instrumentation (LC, LC-MS, IC, IC-MS, GC, GC-MS, ICP-MS, ICP-OES), ICP-MS, trace metals, and cleanroom experience strongly preferred

- Advanced computer knowledge, including MS Office; LIMS experience preferred

- Knowledge and demonstration of proper safe handling/disposal of chemicals and ability to maintain a clean and safe workspace

- Proven record of completing lab work safely, correctly, efficiently, timely, and independently

- Expand upon personal job knowledge by participating in educational opportunities, special project teams, and reading technical publications

- Ability to multi-task and balance independent, teamwork, and time effectively

- Dedication to meticulous attention to detail and organization

- Strong dexterity, good eye-hand coordination, and ability to safely perform routine repetitive motions

- Advanced mechanical inclination and experience operating electrical and nonelectrical laboratory equipment

- We are looking for a first shift Mon-Fri, Weekends/Holidays as needed

**Why Work at Entegris**

Lead. Inspire. Innovate. Define Your Future.

Not everyone who works for a global company shares the same background, experiences and perspectives. We leverage the differences of our employees to bring new ideas to the table. Every employee throughout the company is encouraged to share input on projects and initiatives. Our decision-making process is truly a collaborative effort as we realize there are leaders at every level of the organization. We put our values at the core of how we operate as an organization - not just when it's convenient, but in a lasting and meaningful way. We want the time and energy you spend here to have a positive impact on your life inside and outside of the office

**What We Offer**

Our total rewards package goes above and beyond just a paycheck. Whether you're looking to build your career, improve your health, or protect your wealth, we offer generous benefits to help you achieve your goals.

- Generous 401(K) plan with an impressive employer match

- Excellent health, dental and vision insurance packages to fit your needs

- Flexible work schedule and 11 paid holidays a year

- Paid time off (PTO) policy that empowers you to take the time you need to recharge

- Education assistance to support your learning journey

- Values-driven culture with colleagues that rally around People, Accountability, Creativity and Excellence

Entegris does not provide immigration-related sponsorship for this role. Do not apply for this role if you will need Entegris immigration sponsorship (e.g., H1B, TN, STEM OPT, etc.) now or in the future.

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements, and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status.

Scientist II, Analytical Chemistry

TALENT Software Services is a Service Disabled Veteran-Owned Small Business (SDVOSB) providing the best IT Consulting and Professional Services nationwide for over 35 years. We are one of the most trusted partners for delivery of Project, Data Management, Application, and Infrastructure Services,  TALENT staffs technologies including Java, .NET, Project Management, Analytics, Architecture, and more. 

Representation that counts:  This is where top Twin Cities TALENT find their value in the local marketplace.

"It's easy to get the job done when you're surrounded by TALENT! "

Industry: IT Services and IT Consulting
Company Size: 51-200 employees

TALENT Software Services

**Qualifications**

-  BA/BS (6 yrs.) of relevant experience in analytical chemistry or biologics testing lab

-  MS (4 yrs.) of relevant experience in analytical chemistry or biologics testing lab

-  Ph.D. (1-2 yrs.) of relevant experience in analytical chemistry or biologics testing lab

**Required Skills And Experience**

-  Must have separations experience for large molecules or plate-based assay experience.

-  Experience in analyzing biologics including monoclonal antibodies and/or other therapeutic proteins using at least one of the following techniques:

- Liquid Chromatography (HPLC / UPLC)

- Protein A Titer, Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX, AEX, CEX), Reverse Phase (RP), or Hydrophobic interaction chromatography (HIC)

- Electrophoretic methods such as capillary electrophoresis sodium dodecyl sulfate (CE-SDS) and/or capillary isoelectric focusing (cIEF)

-  Basic instrumentation troubleshooting

-  Ability and willingness to train and follow laboratory methods and procedures

-  Familiarity with Microsoft Office Applications (Outlook, Excel, Word, PowerPoint, OneNote, Teams, etc.)

-  Making accurate reagent preparations (dilutions / solutions / buffers / mobile phases)

-  Good documentation practices & utilization in electronic lab notebooks (ELN)

**Desired Skills And Experience**

-  Analytical software such as Empower.

-  Experience in analyzing biologics including monoclonal antibodies and/or other therapeutic proteins using plate-based methods, e.g., ELISA (HCP, proA)

-  Familiarity with compendial testing such as UV 280, pH, and Physical Observations

Notes:

-  Open to bachelor, masters, and/or PhD level.

-  100% onsite lab based role.

-  Required to have direct expertise in operating LC and CE analytical systems for testing large molecules in an industry or CRO environment.

-  Required to be experienced in the industry, with ability to quickly train on ***-specific procedures and start working in the lab.

-  Role will involve high volume sample testing across multiple preclinical and clinical stage biologics programs, including proteins and antibody-drug conjugates.

-  Required to follow all safety, compliance and quality practices.

-  Required to understand and follow good documentation practices within an electronic laboratory notebook.

-  Required to have strong communication skills, ability to collaborate, and ability to work independently.

**Description**

Support of routine Biologics analytical testing of samples from cell-line development, in-process, process development/characterization, forced degradation, release & stability, and pre-formulation.

**Responsibilities**

-  Support of high-throughput, pre-formulation, pre-qualification, robustness, or admixture testing

-  Results processing and documentation by following appropriate methods / protocols / procedures

-  Sample management and monitoring of controlled temperature units.

-  Following all appropriate laboratory safety and hygiene procedures.

Scientist - II (Associate)

When progress demands experience, that’s where we come in. 

Yoh is in the business of moving things forward: projects, people, and possibility, delivering the expertise, methodology, and momentum that keep work moving.

From consulting and staffing to enterprise workforce solutions, we bring the expertise to move your business ahead, today and for decades to come. Everything’s aligned and integrated to client needs. 

If it’s powered by science, built by engineers, or driven by data, Yoh is there, embedded in the workforce solutions that move industries ahead. We partner with innovators and problem-solvers who are transforming the marketplace from the inside out. By combining domain expertise with delivery discipline, we turn complex ideas into measurable outcomes.

Nearly a century after our founding, Yoh remains STEM-centered, values-charged, and fully focused on improving business operations and outcomes. Yoh works wherever progress moves fast, with: industries defined by innovation, compliance, and transformation. Our flexible, scalable approach helps the world's best and brightest companies deliver impact. Yoh is a proud member of the Day & Zimmermann family of companies.

Industry: Staffing and Recruiting
Company Size: 1,001-5,000 employees

Yoh, A Day & Zimmermann Company

**Analytical Chemist**

**St. Louis, MO or Durham, NC - ONSITE**

**1 Year W2 contract (with potential to extend or transition to perm)**

**Pay rate: $35-43/hr - Depending on Education and Experience**

**MUST HAVE QUANTITATIVE METHOD DEVELOPMENT WITH LC-MS/MS**

**Shift: **First Shift

**Summary: **

- Participate and assist in planning and conducting activities to develop new products or methods/techniques within the Clinical Microbiology product portfolio in full compliance with current quality and safety standards

- Provide technical assistance for activities to improve or support existing products, methods or techniques.

**Responsibilities: **

- Perform routine analytical testing & develop analytical methods based on the product development & support needs by using effective and efficient design control techniques.

- Participates in the execution of validation protocols.

- Operate, maintain, and troubleshoot lab equipment including: Sciex LC-MS/MS, Agilent HPLC-UV-ELSD, Thermo IC.

- Responsible for an accurate data analysis process. Plans, evaluates, solves issues, collects data and as well as contributes to the interpretation of results together with team, and deduces further work to be carried out. Prioritizes activities to meet deadlines

- Provide technical input and design standard experiments to optimize experimental performance or investigate failure mode to support operations for existing products, methods, or techniques.

- Creates and presents reports on conducted experiments.

- Performs scientific publications watch and stays informed of the latest advances of a specific expertise area. Contributes to scientific publications.

- Contributes to continuous improvement initiatives.

- Follow company health & safety policies for using chemicals and disposal of chemical waste.

**Skills or Requirements: **

- Bachelors Degree

- Method development with LC-MS and MS REQUIRED

- Proficient in Microsoft Word & Excel required

- Knowledge of cGMP and FDA regulations.

- Good oral and written communications skills in English

- Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment with attention to detail

- Achievement oriented individual possessing intellectual curiosity

- Flexible with ability to work independently to achieve goals while working apart from direct supervision

**What’s In It For You?**

We welcome you to be a part of one of the largest global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you.

- Medical, Dental & Vision Benefits

- 401K Retirement Saving Plan

- Life & Disability Insurance

- Direct Deposit & weekly ePayroll

- Employee Discount Programs

- Referral Bonus Programs

**Estimated Min Rate **: $29.40

**Estimated Max Rate **: $42.00

**What’s In It for You?**

We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

- Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)

- Health Savings Account (HSA) (for employees working 20+ hours per week)

- Life & Disability Insurance (for employees working 20+ hours per week)

- MetLife Voluntary Benefits

- Employee Assistance Program (EAP)

- 401K Retirement Savings Plan

- Direct Deposit & weekly epayroll

- Referral Bonus Programs

- Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit **https://www.yoh.com/applicants-with-disabilities ** to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: **https://www.yoh.com/privacy-notice **

HuFriedyGroup is a global leader in dental instrument manufacturing, infection prevention and instrument reprocessing workflows. With over 200 years of collective experience in the dental industry, HuFriedyGroup helps dental professionals be the best in practice by providing a complete circle of protection in the dental suite, bringing together world class products, services, education, and communities that result in superior clinician performance, superior clinical outcomes, and safety for clinicians and patients. Headquartered in Chicago, HuFriedyGroup products are distributed in more than 100 countries, and the dental division maintains offices in Germany, Italy, China, Singapore, and Japan.

Industry: Medical Equipment Manufacturing
Company Size: 1,001-5,000 employees

HuFriedyGroup

**Job Title: ** Laboratory Technician I

**Please note this is a full-time permanent position and not a seasonal summer job.**

**Join Our Team at HuFriedyGroup – Innovating Excellence in Dental Instrument Manufacturing**

At HuFriedyGroup, we are committed to providing high-quality dental instruments to organizations and professionals worldwide. We value innovation, craftsmanship, and dedication to improving oral health outcomes globally. Our people are our strength, and we foster a collaborative environment where every team member can thrive. When you join HuFriedyGroup, you become part of a company that truly values YOU, and we are committed to investing in your future both professionally and personally. We offer competitive salaries, comprehensive healthcare benefits, tuition assistance, generous paid time off, holidays, a matching 401(k), and annual merit and incentive plans.

**Job Summary: **The laboratory Technician position performs assigned laboratory procedures, including data entry, processing, and resulting of biological indicator spore strip tests.

- Aseptic transfer of tests, categorizing incoming customer tests, performing Gram stain technique to verify positive test results

- Maintain accurate customer records

- Follows the laboratory procedure for testing samples including

- Sorting envelopes into single and double strips packs

- Label the envelopes and perform data entry

- Transferring of spore strips

- Pulling and recording of positive samples

- Various day-to-day preparation of lab supplies

- Proficient at property software

- Adheres to Laboratory quality control policies

- Identifies problems that may adversely affect test performance or reporting of test results

- Establish and maintain effective working relationships

- All other assigned duties including

- Opening mail

- Cleaning of laboratory and office areas

- Mail pick-up and counting

- Restock supplies

- Prep gram stains and view positives

- Archive transferred envelopes

**Benefits**

Healthcare, Vision, Dental, Quarterly Bonuses, 401K Match, PTO, Company Holidays

**Preferred Experience**

- 1+ years’ related experience and/or training, or equivalent combination of education and experience in a laboratory operation or technical/scientific field, and basic computer competency is required.

- Some knowledge of aseptic laboratory techniques, and microscope familiarity is preferred

- Requires attention to detail, manual dexterity, well-focused, sense of urgency, good work ethic, and ability to function as part of a team

**Required Education/ Degree**

At HuFriedyGroup, we understand that valuable skills and experience come from all walks of life. If you don’t have a college degree or high school diploma, don’t worry—it won’t disqualify you from being considered for this role. We value the unique perspectives and abilities you bring to the table.

**Equal Employment Opportunity & Accessibility Statement**

HuFriedyGroup is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We prohibit discrimination and harassment of any kind based on race, color, religion, age, gender, national origin, disability status, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

If you require reasonable accommodations to apply for a position, participate in the recruitment process, or perform essential job functions, please contact us at 773-868-5534. We are committed to supporting you throughout your journey with HuFriedyGroup!

1st Shift: Monday-Friday, 7:30am-4:00pm

Culture Laboratory Technician I

Mission Statement

Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.

Responsibilities*

**Provide Clerical/Administrative Support**

- Answer telephone calls

- Scan documents (scan requisitions and worksheets); organize and file test reports and documents, file slides

- Manage inventory: unpack shipments, stock lab supplies, reconcile invoices

- Assist with training new staff, House Officers, and faculty as appropriate

**Accessioning, Specimen Processing And Distribution**

- Track specimens/assets to receive and send specimens between departments.

- Accession, process and distribute patient samples within the laboratory consistent with accuracy and quality assurance goals of the laboratory.

- Access and navigate the Pathology Document Control System, Hospital Information System (HIS), and Laboratory Information System (LIS) to accession patient specimens, requesting additional information from appropriate resources.

- Assist in Problem solving (duplicate scan requests, missing slides, incorrect slides, and missing information); call on unacceptable specimens (misaligned coverslips, excess medium, broken slides etc.).

- Work with other Digital Pathology, Histology, or Cytology laboratory personnel to process and/or store patient casework with optimal efficiency and accuracy (e.g. basic

- sample preparation and setup of assays, loading instrument or automation lines, filing of slides and blocks).

**Maintain and Operate Instruments*/Laboratory Support:**

- Perform and document daily maintenance as specified in instrument procedures.

- Analyze patient samples/slides as specified in the instrument procedures.

- Enter information into laboratory databases or picture archive communication systems (PACS).

- Ensure continuous operation by routinely monitoring the status of reagents, parts and supplies.

- Monitor error codes and perform basic troubleshooting. Notify a supervisor or senior operator if unable to resolve an instrument problem. Document problems, action taken and outcomes in instrument log books.

- Operate the dishwasher and autoclave to clean and sterilize laboratory supplies; wash slide cassettes. Prepare reagents. Maintain work area in a well-stocked, clean condition.

**Perform Testing**

- Perform analysis of quality control material with documentation of completion and of action taken for out-of-range values.

- Accurately transfer off-line patient data from worksheets and instrument printouts to the computer/LIS/PACS

**Professional Development**

- Fulfill departmental continuing education requirement.

**Characteristic Duties And Responsibilities**

- Track the inflow of glass slides for whole slide imaging

- Prioritize urgent scanning requests

- Appropriately clean, organize and prepare microscope slides containing histologically mounted tissue for scanning (whole-slide imaging)

- Appropriately judge the quality of scanned images

- Recognize and resolve basic hardware or software problems. Work through unique issues with additional staff/supervisor as needed

- Recognize any workflow irregularities/inconsistencies and take appropriate action on his/her own initiative. Work through unique issues with additional staff/supervisor as needed.

- Must be able to operate and interact with both our vendor-supplied and custom software and database

- Track the return of glass slides to clients

- Deliver glass slides as needed

- Assist with management of image storage resources

- Interact with faculty and trainees regarding special whole-slide imaging requests, escalate to supervisor if required; perform customized workflows as directed

- Travel to enterprise sites where unit-related functions and instruments are located to perform training or troubleshooting

- Participate in training on new or additional instruments, workflow updates or changes, software implementation and changes, and telepathology systems

- Perform instrument verification following repairs or moves and record results Observe all procedures for protected health information (PHI) On occasion, perform scanning of photographs, negatives, or color film transparencies

Required Qualifications*

**In order to be considered for this position the applicant must have met or will have met all the required qualifications prior to the start date of employment.**

- High school diploma

- Requires frequent standing/walking/sitting for long periods of time and the ability to lift up to 25lbs.

Desired Qualifications*

- One or more years college instruction or associate degree or equivalent experience with exposure to biology, anatomy and physiology, or other laboratory related field Reasonable knowledge of the methods, materials and equipment used in laboratory activities is desirable.

- Previous experience in performance of standard laboratory procedures

- Demonstrated confidence and ability with computers and software

- Attention to detail

- Willing to work in a growing and rapidly changing environment

- The ability to prioritize tasks under occasional high work volumes without sacrificing accuracy

- Excellent communication skills

Why Join Michigan Medicine?

Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.

**What Benefits can you Look Forward to?**

- Excellent medical, dental and vision coverage effective on your very first day

- 2:1 Match on retirement savings

Modes of Work

Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.

Work Schedule

This full time, 40 hour position is on the night shift and will require rotating holidays and weekends and on-call.

Additional Information

- Works with infectious disease and/or hazardous materials

- May have exposure to noise from laboratory equipment and pneumatic tube system.

Union Affiliation

This position is covered under the collective bargaining agreement between the U-M and the United Michigan Medicine Allied Professionals (UMMAP), which contains and settles all matters with respect to wages, benefits, hours, and other terms and conditions of employment.

Background Screening

Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.

Application Deadline

Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.

U-M EEO Statement

The University of Michigan is an equal employment opportunity employer.

Laboratory Technician

At Camin Cargo, we provide inspection, laboratory testing, and additive treatment solutions to the Petroleum Industry. With 67 branches serving key ports and blending hubs across North, South, and Central America, the Caribbean, and Europe, we have been providing ethical, reliable, and comprehensive service for over 40 years. 

Our focus is maintaining the highest level of service, quality, and customer satisfaction throughout our industry as we continue to grow our presence. To perform at the highest standards, we are continuously evaluating our services to meet and surpass the growing demands required by our clients. 

We are proud to institute the highest level of business responsiveness to achieve efficient, adaptive performance in today’s energy sector. Our expertise covers the oil and gas, petrochemicals, renewables (including biofuels, RD and SAF), and agriculture markets. 

As your independent third-party inspection provider, we determine and certify quantity and quality for custody transfers of bulk liquid, gaseous, and dry cargoes. The qualities of our field staff are mirrored and complemented by our operations team and laboratory staff.  

Our inspection and laboratory services are performed with strict adherence to the latest American Petroleum Institute (API) and American Society for Testing and Materials (ASTM) standards, government regulations, and industry protocols. 

Bonded with U.S. Customs and Border Protection 
ISO 9001:2000 Certified 
ISO 17025:2005 Accredited 
BQ 9000 Certified 
EPA registered for Fuels Testing 
Approved by the New York Mercantile Exchange 
Active members of ASTM, API, EI, IFIA, ASQ, GAFTA, FOSFA, ISO, AOCS and ACS

Industry: Oil and Gas
Company Size: 1,001-5,000 employees

Camin Cargo Control Inc.

**Laboratory Technician I **

**Company Overview **

Camin Cargo is a leading provider of inspection, testing, and certification services in the oil and gas industry. We are committed to ensuring the highest standards of safety, quality, and compliance for our clients worldwide. We are seeking an energetic Laboratory Technician I to join our team.

**Position Summary **

The Laboratory Technician I is responsible for conducting routine laboratory tests and analyses on various samples related to crude oil, refined products, and petrochemicals. This entry-level position requires attention to detail, adherence to safety standards, and the ability to accurately document test results.

**Responsibilities **

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

- Perform routine laboratory tests and analyses on crude oil, refined petroleum, petrochemical products, and quality control samples.

- Record test results, input data, and analyze findings for review by senior laboratory staff or management.

- Ensure that all samples are accurately labeled and documented for traceability and regulatory compliance.

- Enter test results and data into the company’s internal software systems for tracking and reporting purposes.

- Follow safety protocols and best practices for handling hazardous materials and operating laboratory equipment.

- Assist in maintaining and organizing the laboratory inventory.

- Support senior technicians and lab supervisors in specialized testing as needed.

- Contribute to maintaining the cleanliness and orderliness of the laboratory.

- Participate in training sessions and professional development opportunities as required.

- All other job duties as defined.

**Minimum Requirements **

- Associate's degree in a relevant field (Chemistry, Chemical Engineering, or a related science preferred).

- 0-2 years of experience in a laboratory setting, preferably in the oil and gas industry.

- Knowledge of laboratory safety procedures and practices.

- Strong attention to detail and ability to handle multiple tasks.

- Ability to follow instructions accurately and work under minimal supervision.

- Good written and verbal communication skills.

- Visual acuity to interpret test results and operate laboratory instruments.

- Proficient in Microsoft Office Suite (Word, Excel, Outlook).

- Ability to learn new software systems and applications specific to the company's internal processes.

- Must be able to work effectively both independently and as part of a team.

**Fitness for Duty – Physical Demands **

- The position requires prolonged periods of standing and walking during sample preparation, testing, and equipment calibration.

- Ability to lift and carry up to 30 pounds, such as chemical containers or laboratory equipment.

- Working in varying environmental conditions, including exposure to chemicals and laboratory hazards, while adhering to safety protocols.

- Ability to wear personal protective equipment (PPE), including gloves, safety glasses, lab coats, and respirators, as necessary.

This document contains Confidential and Proprietary information which is the property of Camin Cargo Control.  None of the information contained herein may be disclosed, reproduced, distributed, or used without prior written consent from Camin.   All rights reserved.

Laboratory Technician - I

UES provides personalized engineering, environmental, testing and inspection services to clients across the United States. We’re experts in the areas of environmental and earth sciences, sustainable infrastructure solutions, and geophysical technologies.

WHAT WE DO
Our experts identify and solve complex engineering and construction challenges by providing clients with innovative, technology-based solutions. Our goal is to support the design and construction of sustainable infrastructure solutions from development to redevelopment. 

WHO WE SERVE
With nearly 4,000 professionals across 85+ branches, UES consults on projects of all sizes for public and private clients in industries such as transportation,  infrastructure, water and wastewater, technology, power transition, healthcare, education, industrial, residential, and more.

OUR PROJECTS
We’ve successfully completed hundreds of thousands of projects across the country including work on solar farms, electric battery plants, data centers, roadways, bridges, water reservoirs, hospitals, schools, stadiums, airports, hotels and resorts, residential homes, and more.

Industry: Engineering Services
Company Size: 1,001-5,000 employees

**Overview**

~~At UES, we’re a team of more than 4,000 engineers, scientists, geologists, inspectors, technicians, and drillers united by a shared purpose—to make a meaningful impact in the communities we serve. As a national leader in geotechnical engineering, environmental consulting, and materials testing and inspection, we collaborate on transformative projects across transportation, energy, water, healthcare, and more. Learn more about the benefits of joining Team UES and our core values at careers.teamues.com.~~

**Position Overview**

We are seeking a detail-oriented and motivated Laboratory Technician I to join our team and support geotechnical, construction materials testing, and environmental projects. This role is responsible for performing laboratory testing and analysis on soil, concrete, asphalt, aggregates, and other construction materials to ensure compliance with industry standards and project specifications. Working in a controlled laboratory environment, the Lab Technician I plays a vital role in ensuring accurate, high-quality test results that support infrastructure and construction projects.

The ideal candidate will have a strong attention to detail, the ability to follow standardized testing procedures, and a commitment to safety and quality assurance. You will be responsible for preparing samples, operating and maintaining testing equipment, recording data, and assisting in maintaining laboratory organization and compliance.

**Responsibilities**

- Perform routine laboratory testing on construction materials, including soil, concrete, and other construction materials following ASTM, AASHTO, and other applicable industry standards to ensure compliance with project specifications.

- Ensure that project testing requirements are met and compliant with project specifications, requirements, and company policies and procedures.

- Accurately document and report test results, maintaining detailed, organized, and error-free records.

- Assist with sample preparation, handling, and proper storage, ensuring sample integrity, traceability, and adherence to laboratory protocols.

- Operate laboratory testing equipment.

- Follow strict safety protocols and laboratory procedures, including proper handling of materials and use of personal protective equipment (PPE).

- Communicate effectively with lab supervisors, engineers, and field personnel, providing timely updates on test results, sample status, and any technical issues.

- Perform additional duties as assigned, supporting the laboratory team, field technicians, and project managers as needed.

**Qualifications**

- High school diploma or equivalent required; associate degree or technical coursework in engineering, geology, construction science, or a related field preferred.

- 0-3 years of experience in construction materials testing, geotechnical laboratory work, or a related field (prior laboratory experience preferred but not required).

- Commitment to workplace safety, following OSHA, company, and laboratory safety protocols, including the proper use of personal protective equipment (PPE).

- Basic computer proficiency, with experience in Microsoft Office (Excel, Word, Outlook) and Field Data Collection (FDC) software preferred.

- Ability to read, write, and interpret procedures, manuals, technical documents, and reports related to construction materials testing and laboratory protocols.

- Mathematical skills sufficient to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.

- Effective verbal and written communication skills, with the ability to collaborate with colleagues, supervisors, field personnel, and clients to carry out instructions and report findings.

- Strong organizational, time management, and problem-solving skills, with the ability to manage multiple tasks efficiently.

- Detail-oriented and quality-focused, ensuring accuracy in sample preparation, testing procedures, and data documentation.

- Ability to work independently within the limitations of experience, using initiative to solve routine lab challenges.

- Ability to stand for extended periods of time and perform physically demanding tasks, including lifting and moving materials or equipment.

- Valid driver’s license with an acceptable driving record; ability to travel to job sites as needed.

**Travel Requirements**

- This position does not require regular travel as part of its primary responsibilities. However, occasional

travel may be required, up to 10%, primarily for occasional off-site meetings, training sessions, or

company events. Travel, when necessary, will be communicated in advance and aligned with business

needs.

**Physical Demands & Work Environment**

Work is sometimes conducted in a laboratory setting, but may also involve fieldwork and exposure to outdoor conditions, including:

- Sites that may not be accessible by vehicle, requiring travel on foot through wetlands, swamps, grasslands, construction zones, and other uneven or rugged terrain with natural and man-made obstacles such as sand, brush, and debris.

- Moderate to loud noise levels due to lab equipment, field operations, and construction environments.

- Exposure to dirt, dust, chemicals, sun, heat, humidity, and varying weather conditions as part of field sample collection and testing.

Physical requirements include:

- Ability to lift and carry between 35 and 75 lbs. over distances up to 75 feet, involving regular repetitive motion.

- Ability to stand, walk, drive, and operate laboratory and field equipment for extended periods.

- Frequent use of hands and arms for typing, handling samples, operating lab instruments, and performing testing procedures.

- Ability to bend, twist, reach, stoop, pull, kneel, climb, balance, lift, carry, and push as required for laboratory and fieldwork.

- Ability to communicate effectively through verbal and written means in a lab and field environment, often requiring the use of PPE (Personal Protective Equipment).

- Ability to use your senses to see (including close, distant, and peripheral vison, depth vision, and ability to focus) and smell.

**EEO Statement**

**UES is an Equal Opportunity Employer and is proud to recruit the most qualified candidates. Please see our full EEO Statement at the bottom of the page ****here **

Laboratory Technician I

NeoGenomics, Inc. specializes in cancer genetics testing and information services, providing one of the most comprehensive oncology-focused testing menus in the world for physicians to help them diagnose and treat cancer. The Company’s Advanced Diagnostics Division serves pharmaceutical clients in clinical trials and drug development.

NeoGenomics is committed to connecting patients with life altering therapies and trials. We believe that, together, with our partners, we can help patients with cancer today and the next person diagnosed tomorrow. In carrying out these commitments, NeoGenomics adheres to relevant data protection laws, provides transparency and choice to patients regarding the handling and use of their data through our Notice of Privacy Practices, and has invested in leading technologies to secure the data we maintain.

Headquartered in Fort Myers, FL, NeoGenomics operates CAP accredited and CLIA certified laboratories for full-service sample processing in Fort Myers, Florida; Aliso Viejo and San Diego, California; Research Triangle Park, North Carolina; and Houston, Texas; and a CAP accredited full-service, sample-processing laboratory in Cambridge, United Kingdom. NeoGenomics also has several, small, non-processing laboratory locations across the United States for providing analysis services. NeoGenomics serves the needs of pathologists, oncologists, academic centers, hospital systems, pharmaceutical firms, integrated service delivery networks, and managed care organizations throughout the United States, and a pharmaceutical firm in Europe.

Industry: Hospitals and Health Care
Company Size: 1,001-5,000 employees

NeoGenomics Laboratories

Are you motivated to participate in a dynamic, multi-tasking environment? Do you want to join a company that invests in its employees? Are you seeking a position where you can use your skills while continuing to be challenged and learn? Then we encourage you to dive deeper into this opportunity.

We believe in career development and empowering our employees. Not only do we provide career coaches internally, but we offer many training opportunities to expand your knowledge base! We have highly competitive benefits with a variety of HMO and PPO options. We have company 401k match along with an Employee Stock Purchase Program. We have tuition reimbursement, leadership development, and even start employees off with 16 days of paid time off plus holidays. We offer wellness courses and have highly engaged employee resource groups. Come join the Neo team and be part of our amazing World Class Culture!

NeoGenomics is looking for a Laboratory Technician I for our FISH department in Aliso Viejo, CA who wants to continue to learn in order to allow our company to grow.

~~Shift: Sunday-Thursday, 8:00am-4:30pm (subject to change based on business needs) ~~

Now that you know what we're looking for in talent, let us tell you why you'd want to work at NeoGenomics:As an employer, we promise to provide you with a purpose driven mission in which you have the opportunity to save lives by improving patient care through the exceptional work you perform. Together, we will become the world's leading cancer reference laboratory.

Position Summary:Under the direct supervision of licensed personnel, or within a training environment, the Laboratory Technician will assist with responsibilities associated with processing specimens for clinical testing and will provide general support for the laboratory following established policies and procedures.

This is the entry level for the Laboratory Technician job category. The employee works in a learning capacity while performing a range of laboratory technician assignments under close supervision.

Responsibilities:

- Receives, organizes and processes clinical specimens accurately. Identifies worksheet, computer, and specimen problems and demonstrates ability to either resolve or elevate to licensed personnel appropriately

- Prepares and organizes written data, printouts, and other documents for licensed technologist to review

- Prepares testing equipment, assists with preventative maintenance

- Reports problems concerning individual tasks, equipment, and supplies to the Laboratory Supervisor or the Lead Technologist to ensure timely resolution

- Operates automated equipment per SOP

- Prepares reagents and controls using automated or fixed measuring devices following established SOP’s. Maintains complete and accurate records of reagents

- Responds promptly to pathologists, managers/supervisors/lead, technologists, and administrative requests

- Read and understand all SOP’s related to the department and adhere to all department rules and protocols

- Logging of Quality Control and Quality Assurance results for review by licensed technologist and supervisor’s monthly signoff

- Assists in preparation of validation documentation preparation for new tests and procedures as required by the company, following manufacturer’s guidelines or SOP’s established by the Company

- Maintain laboratory in a clean, functional state, as well as cleaning or performing / scheduling equipment and instrument maintenance, as required

- Demonstrates initiative in making suggestions to improve efficiency and productivity and provides consistent feedback

- Attends department meetings and company in-service trainings to enhance knowledge on testing and systems

Experience, Educations and Qualifications:

- BS or BA degree is required (in a life or physical science field is strongly preferred) / or AA or AS degree in conjunction with Medical Laboratory Technician License

- 1+ years of experience equivalent to a Laboratory Technician or Laboratory Assistant preferred

- Certification Compliance Requirements:FL: State of Florida Trainee License, or Medical Laboratory Technician LicenseCA: Bachelor’s degree required; No license requiredTN: State of Tennessee Trainee License, Temporary License, or Medical Laboratory Technician License

- Basic understanding of laboratory techniques preferred

- Basic understanding of MS Office programs

- Ability to communicate effectively

- Strong organizational skills and attention to detail

- Ability to work independently

- Must be able to work in a fast paced, multi-tasking environment and maintain production and quality standards

- Must be able to work in a biohazard environment and comply with safety policies and standards outlined in the Safety Manual

- Must be able to lift up to 50 pounds

Laboratory Technician I - FISH

At Joulé, we believe our world is filled with possibilities – where character, integrity, and commitment drive our purpose. For over 30 years, Joulé has been a trusted partner to industry-leading clinical, scientific, and healthcare organizations by providing innovative workforce solutions and delivering top talent. Operating at the forefront of the life sciences arena, Joulé’s relentless approach enables our clients to rapidly and effectively execute critical initiatives and major projects. Joulé is a System One division.

Industry: Staffing and Recruiting
Company Size: 51-200 employees

Joulé

**Job Title: **           Laboratory Technician

**Location: **          Hunt Valley, MD

**Schedule: **         Day Shift - 8am-5pm

**Type: **               3 month contract, possible extension

**Start: **            ASAP

**Responsibilities:**

- Perform testing on various samples assigned to the laboratory team.

- Keep proper data documentation for all samples.

- Monitor laboratory inventory and share any inventory needs with the team.

- Follow all standard laboratory procedures.

**Requirements:**

- Bachelor’s degree in life science; Chemistry strongly preferred.

- Laboratory experience in a chemistry setting; academic laboratory experience accepted.

- Experience with gas chromatography, automatic titrators, pH testing, pipetting, and UV-Vis strongly preferred.

- Ability to communicate both verbally and electronically.

Ref: #558-Scientific

Mission Statement

Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.

Responsibilities*

**BASIC FUNCTION RESPONSIBILITY**

- Perform the assigned duties in Specimen Processing & Send out Lab to assure accurate and timely receipt, order entry, transport, processing, and distribution of laboratory specimens. Provide excellent customer service to internal and external customers. Have the ability to coordinate the activities of all the Specimen Processing staff on all shifts in order to assure accurate and timely processing of laboratory specimens and customer service support in the absence of supervision.

- Work with a high level independence & excellence.

**Characteristic Duties Responsibilities**

**Receive, OE, Process & Distribute, UMHS, MLABS & Send outs:**

- Must complete training and be checked off on all benches and be scheduled for sendout training by training specialists. If training is unable to be scheduled must have knowledge of processing of 60% of send out specimens.

- Maintain knowledge base to perform all MLabs specimen processing

- Function with independence on all benches assigned

- Prepare specimens for reference labs including FedEx packaging

- Scan documents to patient files

- Identify, report and correct problems

- Order Entry of Send out tests to SOFT and Reference labs systems

**Customer Service**

- Provide total customer focus to meet the needs of every customer, internal (including co-workers) and external, including medical staff, laboratory staff, MLABS clients, patients, and families.

**Quality Control**

- Maintain quality control as required for Specimen Processing; including temperature checks on all storage refrigerators and freezers, daily Q.A. of Send out requisitions and other Q.C. projects as assigned.

**Safety**

- Comply with all safety procedures/instructions and observe safe work practices. Practice all BSP standards for your unit/department. Serve as a role model.

**Communication And Teamwork**

- Use effective communication including written, verbal, and information technology skills. Work effectively with staff to accomplish goals.

**Leadership**

- Model professional behaviors.

- Serve as a resource for Specimen Processors and other departmental staff.

- Fill in as the go to person in the absence of an Associate Supervisor or the Unit Supervisor.

**In the absence of a supervisor must be able to:**

- Check for call-ins or changes to schedule and make adjustments as needed, also notify those affected by the change

- Ensure all staff duties are covered (sweeps, lab assignments, benches, etc.)

- Be available for new hires for questions and concerns

- Continuously monitor workflow making assignment adjustments as need

- Determine appropriate break/lunch times to ensure optimum staffing is maintained at all times

- Determine appropriate work partners to maximize staff skill set

- Ensure staff is prioritizing appropriately

- Knowledge of the mislabel procedure and gather all documentation for supervisor

- Knowledge of procedure for MiChart problems (ext 68000)

- Knowledge of Pathtrack, Soft issues and contact information (PI ext 66740)

- Functional Assistance: Assist with special projects, in-services, huddles, evaluating new equipment and techniques, review procedures, and other additional responsibilities as assigned.

**Training**

- Assist Training Specialist and Associate Supervisor as a preceptor for training new employees as needed or requested

**Mandatories, Continuing Education, Competencies And Training**

- Complete yearly departmental mandatories as required. Attend departmental, assigned and/or requested continuing education training, classes, etc.

- Complete monthly, quarterly, or yearly competencies as assigned

- Comply with ongoing training for the unit and department

**Supervision Received**

- Supervision is received from the Associate Supervisor, Training Supervisor, Senior Clinical Technologist, Allied Health Supervisor, the Specimen Processing Manager, or other designated official.

**Supervision Exercised**

- Function as a Team Leader (as requested/assigned) in the absence of an Associate Supervisor/Supervisor.

Required Qualifications*

**In order to be considered for this position the applicant must have met or will have met all the required qualifications prior to the start date of employment.**

- High school diploma

- Science classes at a college level are required.

- Ability to complete all training and testing.

Desired Qualifications*

Preferred: Bachelor's degree in the natural or physical sciences or an equivalent combination of education and experience

Why Join Michigan Medicine?

Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.

**What Benefits can you Look Forward to?**

- Excellent medical, dental and vision coverage effective on your very first day

- 2:1 Match on retirement savings

Modes of Work

Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.

Work Schedule

This full time, 40 hour position is on the evening shift and will include rotating weekends, holidays and on-call.

Union Affiliation

This position is covered under the collective bargaining agreement between the U-M and the United Michigan Medicine Allied Professionals (UMMAP), which contains and settles all matters with respect to wages, benefits, hours, and other terms and conditions of employment.

Background Screening

Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.

Application Deadline

Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.

U-M EEO Statement

The University of Michigan is an equal employment opportunity employer.

**Overview**

~~At UES, we’re a team of more than 4,000 engineers, scientists, geologists, inspectors, technicians, and drillers united by a shared purpose—to make a meaningful impact in the communities we serve. As a national leader in geotechnical engineering, environmental consulting, and materials testing and inspection, we collaborate on transformative projects across transportation, energy, water, healthcare, and more. Learn more about the benefits of joining Team UES and our core values at careers.teamues.com.~~

**Position Overview**

We are seeking a detail-oriented and motivated Laboratory Technician I to join our team and support geotechnical, construction materials testing, and environmental projects. This role is responsible for performing laboratory testing and analysis on soil, concrete, asphalt, aggregates, and other construction materials to ensure compliance with industry standards and project specifications. Working in a controlled laboratory environment, the Lab Technician I plays a vital role in ensuring accurate, high-quality test results that support infrastructure and construction projects.

The ideal candidate will have a strong attention to detail, the ability to follow standardized testing procedures, and a commitment to safety and quality assurance. You will be responsible for preparing samples, operating and maintaining testing equipment, recording data, and assisting in maintaining laboratory organization and compliance.

**Responsibilities**

- Perform routine laboratory testing on construction materials, including soil, concrete, and other construction materials following ASTM, AASHTO, and other applicable industry standards to ensure compliance with project specifications.

- Ensure that project testing requirements are met and compliant with project specifications, requirements, and company policies and procedures.

- Accurately document and report test results, maintaining detailed, organized, and error-free records.

- Assist with sample preparation, handling, and proper storage, ensuring sample integrity, traceability, and adherence to laboratory protocols.

- Operate laboratory testing equipment.

- Follow strict safety protocols and laboratory procedures, including proper handling of materials and use of personal protective equipment (PPE).

- Communicate effectively with lab supervisors, engineers, and field personnel, providing timely updates on test results, sample status, and any technical issues.

- Perform additional duties as assigned, supporting the laboratory team, field technicians, and project managers as needed.

**Qualifications**

- High school diploma or equivalent required; associate degree or technical coursework in engineering, geology, construction science, or a related field preferred.

- 0-3 years of experience in construction materials testing, geotechnical laboratory work, or a related field (prior laboratory experience preferred but not required).

- Commitment to workplace safety, following OSHA, company, and laboratory safety protocols, including the proper use of personal protective equipment (PPE).

- Basic computer proficiency, with experience in Microsoft Office (Excel, Word, Outlook) and Field Data Collection (FDC) software preferred.

- Ability to read, write, and interpret procedures, manuals, technical documents, and reports related to construction materials testing and laboratory protocols.

- Mathematical skills sufficient to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.

- Effective verbal and written communication skills, with the ability to collaborate with colleagues, supervisors, field personnel, and clients to carry out instructions and report findings.

- Strong organizational, time management, and problem-solving skills, with the ability to manage multiple tasks efficiently.

- Detail-oriented and quality-focused, ensuring accuracy in sample preparation, testing procedures, and data documentation.

- Ability to work independently within the limitations of experience, using initiative to solve routine lab challenges.

- Ability to stand for extended periods of time and perform physically demanding tasks, including lifting and moving materials or equipment.

- Valid driver’s license with an acceptable driving record; ability to travel to job sites as needed.

**Travel Requirements**

- This position does not require regular travel as part of its primary responsibilities. However, occasional travel may be required, up to 10%, primarily for occasional off-site meetings, training sessions, or company events. Travel, when necessary, will be communicated in advance and aligned with business needs.

**Physical Demands & Work Environment**

Work is sometimes conducted in a laboratory setting, but may also involve fieldwork and exposure to outdoor conditions, including:

- Sites that may not be accessible by vehicle, requiring travel on foot through wetlands, swamps, grasslands, construction zones, and other uneven or rugged terrain with natural and man-made obstacles such as sand, brush, and debris.

- Moderate to loud noise levels due to lab equipment, field operations, and construction environments.

- Exposure to dirt, dust, chemicals, sun, heat, humidity, and varying weather conditions as part of field sample collection and testing.

Physical requirements include:

- Ability to lift and carry between 35 and 75 lbs. over distances up to 75 feet, involving regular repetitive motion.

- Ability to stand, walk, drive, and operate laboratory and field equipment for extended periods.

- Frequent use of hands and arms for typing, handling samples, operating lab instruments, and performing testing procedures.

- Ability to bend, twist, reach, stoop, pull, kneel, climb, balance, lift, carry, and push as required for laboratory and fieldwork.

- Ability to communicate effectively through verbal and written means in a lab and field environment, often requiring the use of PPE (Personal Protective Equipment).

- Ability to use your senses to see (including close, distant, and peripheral vison, depth vision, and ability to focus) and smell.

**EEO Statement**

**UES is an Equal Opportunity Employer and is proud to recruit the most qualified candidates. Please see our full EEO Statement at the bottom of the page ****here**

In our relentless pursuit of greatness, we are dedicated to developing individuals, creating exceptional teams, and cultivating a unique culture of unity and care. As providers of digital talent solutions, we aim to positively impact businesses and communities globally. We would be honored to be your trusted and uncommon partner on this journey.

Industry: Information Technology & Services
Company Size: 10,001+ employees

Collabera

**Job Summary: **

The Laboratory Technician I supports global laboratory operations with a focus on Laboratory Information Management Systems and quality systems processes. This role involves assisting with document control activities, inventory management, and digital readiness initiatives. The position requires strong coordination with cross-functional and global teams to support laboratory projects and ensure compliance with quality standards.

**Key Responsibilities: **

• Support global laboratory projects related to Laboratory Information Management Systems, including SampleManager

• Assist in creating, updating, and routing document change controls within quality systems

• Collaborate with global quality systems teams to manage administrative updates to procedures and training

• Coordinate with site and global stakeholders to support inventory management requests

• Contribute to digital readiness initiatives and other laboratory-related projects

• Provide general administrative and operational support to laboratory quality systems

• Demonstrate willingness to learn and adapt to evolving project needs

**Required Qualifications: **

• Bachelor’s degree in a scientific discipline or related field

• Experience supporting laboratory operations or quality systems

• Familiarity with Laboratory Information Management Systems

• Ability to follow analytical test methods and standard procedures

• Strong organizational and communication skills

• Ability to work effectively in a remote, cross-functional environment

**Preferred Qualifications: **

• Experience with SampleManager or similar Laboratory Information Management Systems

• Background in laboratory administration or quality systems support

• Experience working in multi-site or global project environments

• Chromatography or laboratory analytical experience

**Benefits: **

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.

**Pay Range: $18/hr to $20/hr **

Entry Level Laboratory Information Management Systems Technician

Radify is a deep-tech, venture-backed company tackling one of the largest and most overlooked gaps in our industrial economy: modern metalmaking. 

Metal is a critical input to trillion-dollar industries – and today, our nation is almost entirely dependent on foreign supply of critical minerals and outdated technology.

We’re here to change that. 

To make metal modern. 

To make it here.

Industry: Technology, Information and Internet
Company Size: 2-10 employees

Radify Metals

At Radify Metals, we’re rethinking how the world makes critical metals.

Our team is building a first-of-its-kind plasma metallization platform that converts metal oxides into high-purity metals through cutting-edge materials science, reactor engineering, and process development. This is an opportunity to work at the frontier of advanced manufacturing, directly shaping a technology platform designed to modernize and reshore critical metal supply chains in the United States.

As an early team member, you’ll join at the ground floor of a fast-moving deep-tech startup, where your work will directly influence our technology, products, and company trajectory. We offer meaningful ownership, rapid upward mobility, competitive benefits, and the rare chance to help define both the science and the company from the earliest stages.

**Position Summary: **

Radify Metals is seeking a detail-oriented and technically skilled Laboratory Technician to support the operation of our proprietary plasma reactors. The ideal candidate will be responsible for executing reactor runs, handling samples, documenting experimental data, and assisting with troubleshooting and maintenance to ensure consistent and safe operations.

**Key Responsibilities: **

- Operate reactor systems according to established protocols and safety procedures, including:

- Preparing/loading/unloading samples

- Monitoring reactor performance during runs and documenting observations in real time

- Managing, organizing, and backing up experimental data files;

- Recording any deviations and observations in the data logs, and,

- Performing routine system checks, calibrations, and basic reactor maintenance, including troubleshooting and repairing reactors as issues arise.

- Collaborate with engineers and scientists to improve process efficiency and reliability

- Maintain a clean, organized, and safe laboratory environment

- Follow all safety guidelines, particularly those related to hydrogen gas and plasma systems

**Required Qualifications: **

- Associate’s or Bachelor’s degree in Engineering Technology, Physics, Chemistry, Materials Science, or a related field (or equivalent hands-on experience)

- Mechanical aptitude and problem-solving ability

- Experience working in a laboratory or technical environment

- Ability to follow detailed procedures and maintain accurate documentation

- Strong observational skills and attention to detail

- Basic computer proficiency, including file management, data entry, and use of standard software tools

**Preferred Qualifications: **

- Experience with plasma systems, vacuum systems, or semiconductor/advanced materials processing equipment

- Familiarity with data acquisition systems or laboratory information management systems (LIMS)

- Basic understanding of electrical, gas handling, or control systems

- Prior experience troubleshooting technical equipment

**Physical Requirements: **

- Ability to stand for extended periods and work in a laboratory setting

- Capability to lift and handle equipment or samples (within reasonable limits)

- Comfortable working with PPE and in environments involving pressurized gases and high-voltage equipment

**Work Environment: **

This role operates on-site in Campbell, CA in a laboratory setting involving hydrogen gas systems, vacuum equipment, and plasma reactors. Strict adherence to safety protocols is required at all times.

**Key Skills: **

- Attention to detail

- Technical troubleshooting

- Data management and organization

- Communication and documentation

- Team collaboration

**Benefits: **

We offer a highly competitive compensation package that includes salary (range: $80,000-$130,000), meaningful early-stage equity ownership, 401(k), comprehensive health coverage, dental and vision insurance, and life insurance. As an early member of the Radify team, you’ll share directly in the value you help create while building your career alongside a company positioned for significant growth.

3M touches virtually every part of your life. Our people and technology make the impossible, possible. Every day we apply our science to enhance people’s lives. This is 3M Science. Applied to Life.™

Industry: Industrial Machinery Manufacturing
Company Size: 10,001+ employees

**Job Description**

**Collaborate with Innovative 3Mers Around the World**

Choosing where to start and grow your career has a major impact on your professional and personal life, so it’s equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers.

**This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.**

**The Impact You’ll Make in this Role**

**Role**

As a Laboratory Technician, you will play a crucial role in conducting various tests and experiments to ensure the performance and quality of 3M’s consumer products. Here, you will make an impact by:

- Performing a wide range of laboratory tests and experiments on consumer products, following established protocols and procedures

- Collecting, analyzing, and interpreting data accurately and efficiently

- Operating, maintaining, and calibrating laboratory equipment to ensure accurate and reliable results

- Preparing samples for testing, adhering to strict safety guidelines

- Using computer software to document and report test results, ensuring accuracy and completeness

- Collaborating with cross-functional teams to troubleshoot and resolve any issues that arise during testing

- Training others on sample preparation, test methods, and lab protocols

**Your Skills And Expertise**

To set you up for success in this role from day one, 3M is looking for candidates who meet following minimum requirements:

- Two-year associate degree or higher in a relevant scientific field (ex: chemistry, biology) from an accredited institution (completed and verified prior to start)

- Minimum of 1 year of experience working in a laboratory setting in a private, public, government or military environment

- Current, valid Driver’s License

Additional qualifications that could help you succeed even further in this role include:

- 2+ years of experience in a laboratory environment, preferably within consumer products or a related industry

- Working knowledge of quality control and quality assurance processes

- Proficiency with statistical analysis tools such as Minitab

- Strong technical troubleshooting, analytical, and problem-solving skills, with the ability to work independently

- Solid understanding of laboratory safety protocols, procedures, and best practices

- Hands-on experience operating laboratory equipment and instrumentation

- Excellent attention to detail, with the ability to follow procedures and instructions accurately

- Strong organizational, time management, communication, and collaboration skills

**Work location: This role follows an on-site working model, requiring the employee to work at least four days a week at the 3M Center in Maplewood, MN.**

**Travel: 0%**

**Relocation: Not authorized**

**Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).**

**Supporting Your Well-being**

3M offers many programs to help you live your best life – both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope.

**Chat with Max**

For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers.

Applicable to US Applicants Only:The expected compensation range for this position is $60,265 - $73,658, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: https://www.3m.com/3M/en_US/careers-us/working-at-3m/benefits/.

Good Faith Posting Date Range 05/19/2026 To 06/18/2026 Or until filled

All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M.

Learn more about 3M’s creative solutions to the world’s problems at www.3M.com or on Instagram, Facebook, and LinkedIn @3M.

Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.

Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement.

Pay & Benefits Overview: https://www.3m.com/3M/en_US/careers-us/working-at-3m/benefits/

3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.

**Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.**

**3M Global Terms of Use and Privacy Statement**

Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms.

Please click on the following links and select the country where you are applying for employment to review the applicable Terms of Use (link here) and Privacy Policy (link here). Before submitting your application, you will be asked to confirm your agreement with the terms.

Lab Technician

Kindred’s mission is to help our patients reach their highest potential for health and healing with intensive medical and rehabilitative care through a compassionate patient experience.

Kindred’s 61 long-term acute care hospitals (LTACHs), along with 18 community-based, short-term acute care hospital campuses from across the nation, became part of ScionHealth with its launch in December 2021. Cornerstone Healthcare Group joined the ScionHealth family of hospitals and hospital services in January 2023. 


In December 2021, Kindred Healthcare became a part of LifePoint Health, a leading healthcare company. As part of this transaction, LifePoint and Kindred also launched a new company, ScionHealth. Today, Kindred’s facilities are now part of either LifePoint or ScionHealth. Specifically, Kindred’s 61 long-term acute care hospitals – along with 18 community-based, short-term acute care hospital campuses from LifePoint – are now a part of ScionHealth.

Industry: Hospitals and Health Care
Company Size: 10,001+ employees

Kindred

**Description**

**Kindred Hospital Chicago - North ** is a 164-bed long-term acute care hospital offering the same in depth care you would receive in a traditional hospital, but for an extended recovery period. We partner with your physician and offer 24-hour clinical care seven days a week so you can start your journey to wellness. To the benefit of our patients, families and visitors, we are located alongside the North Branch Chicago River and surround by the greenery of Horner, Welles and Revere Parks.

**Job Summary**

Clinical Laboratory Assistants (CLAs) perform duties in the laboratory that are above the complexity level of a phlebotomist, but not yet to the level of a medical laboratory technician. They are to collect specimens, do specimen processing, perform limited waived laboratory testing, assist technicians and technologists with maintenance and reagent preparation, plate samples for microbiology, and perform preparation of specimens for testing from alternative laboratory sources.

**Essential Functions**

Verifies test requisitions by comparing information with nursing station log, bringing discrepancies to the attention of unit personnel.

- Verifies patient by reading patient identification. Obtains blood specimens by performing venipunctures and fingersticks.

- Maintains specimen integrity by using aseptic technique, following department procedures, observing isolation procedures.

- Collects therapeutic drug-monitoring assays by collaborating with nursing personnel to ensure appropriate drug dose to collection time.

- Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed.

- Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes.

- Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations.

- Resolves unusual test orders by contacting the physician, pathologist, nursing station, or laboratory testing personnel; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders.

- Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.

- Serves and protects the hospital community by adhering to professional standards, hospital policies and procedures, federal, state, and local requirements, and TJC standards.

- Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.

- Assists with laboratory clerical work. Answers phones, receives specimens and performs preanalytical preparation for samples including send-outs

- Coordinates and actively enhances laboratory workflow by loading instruments, setting up plates, and performing waived testing per laboratory procedures. Performs pending log resolution. Calls critical values to actionable care providers

**Knowledge/Skills/Abilities/Expectations**

- Analyzing Information

- Infection Control

- Bedside Manner

- Attention to Detail

- Lab Environment, Procedural Skills

- Quality Focus

- Hospital Environment, Creating a Safe, Effective Environment

- Performing Diagnostic Procedures

- Approximate percent of time required to travel: 0%

- Must read, write and speak fluent English.

- Must have good and regular attendance.

- Performs other related duties as assigned.

**Pay range: $17.34 - $21.99/Hr**

~~ScionHealth has a comprehensive benefits package for benefit-eligible employees that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.~~

**Qualifications**

**Education**

- Minimum of a High School diploma or Equivalent

**Licenses/Certification**

- Medical Lab Assistant certification preferred but not required.

- State license/registration as required by state.

- Current BLS preferred.

**Experience**

- 1-3 years clinical laboratory experience.

Clinical Lab Assistant - Part-time Days

Industry-leading specialty GI contract research organization (CRO) transforming clinical trial outcomes and accelerating the development of life-changing therapies. We bring together deep GI expertise, advanced medical imaging solutions, clinical operation excellence and cutting-edge precision medicine/laboratory services.

With a global network of 5,000+ sites in >60 countries and growing, we expedite study activation and maximize patient enrollment, ensuring efficient and impactful clinical trials. Trusted by pharmaceutical and biotech partners, we support over 70% of all IBD compounds in development today – delivering customized end-to-end solutions to bring novel therapies to market. 

As a full-service CRO, our offering is tailored to meet your specific clinical research needs:
•	Clinical Trial Services
•	Medical Monitoring
•	Medical Imaging Solutions
•	Medical Research & Development
•	Medical Writing
•	Precision Medicine/Biomarkers
•	Clinical Pharmacology
•	Histopathology via Specialty Lab, AcelaBio
•	Spatial Biology
•	Statistics
•	Real-World Evidence

Headquartered in London, Ontario, Alimentiv operates with globally across Canada, the US, Europe, Asia-Pacific, and Latin America.

Industry: Pharmaceutical Manufacturing
Company Size: 501-1,000 employees

Alimentiv

**About AcelaBio **

AcelaBio is a CAP- and CLIA-accredited specialty histopathology laboratory based in San Diego, CA. We deliver anatomic histopathology, immunostaining, digital image analysis, spatial transcriptomics, and biomarker endpoints to pharmaceutical and biotechnology sponsors. Our team is scientifically driven, client-focused, and committed to advancing translational research through rigorous, reproducible methods.

**About the opportunity **

This is a high-impact, technically hands-on role at the intersection of immunostaining assay development, quantitative image analysis, and client science. You will build and optimize IHC, multiplex IF, and ISH assays from the ground up, develop and maintain AI-assisted image analysis pipelines, and serve as a scientific lead for sponsor studies across preclinical and clinical programs.

You will work directly with pathologists, laboratory technicians, project operations, and business development teams, and will be a visible scientific partner to our pharmaceutical and biotechnology clients. If you are someone who thrives on solving complex assay challenges, values scientific rigor, and enjoys translating data into clear, actionable insights for sponsors, this role is built for you.

**Role Logistics: ** On-site, San Diego (required). Travel expectations : 10%

**Responsibilities **

- **What you'll be doing: **

**Assay Development, Image Analysis (Core Focus): **

- Design, develop, optimize, and validate immunostaining assays including single-plex IHC, multiplex immunofluorescence (mIF), in situ hybridization (ISH), and spatial biology platforms

- Define analytical endpoints, scoring strategies, and QC metrics aligned with assay performance requirements

- Develop, validate, and maintain image analysis pipelines using platforms such as Visiopharm, HALO, or equivalent software

- Build and implement AI/machine learning algorithms for tissue segmentation, cell phenotyping, and biomarker quantification

- Ensure traceability, reproducibility, and thorough documentation of all analysis workflows

- Contribute to assay validation documentation, analytical reports, and regulatory-aligned deliverables

- Partner with histotechnicians to support hands-on assay troubleshooting and knowledge transfer

**Scientific Leadership & Client Engagement; **

- Serve as a scientific interface for sponsors, participating in protocol reviews, study design discussions, and data review meetings

- Provide expert guidance on biomarker study design incorporating omics and non-omics endpoints

- Prepare and review project plans, analysis plans, study reports, abstracts, and technical manuscripts.

- Deliver clear, scientifically rigorous data visualizations, analyses, and summaries tailored to sponsor audiences

**Business Development and Innovation: **

- Support RFP responses, project pricing, protocol review, and bid defense activities

- Contribute to the development of sales, marketing, and promotional scientific content

- Drive continuous improvement of our computational pathology, spatial biology, and translational research service offerings

- Participate in capability development and functionality reviews to expand the AcelaBio service portfolio

**Qualifications **

-

**Education and Experience: **

Graduate degree (M.Sc. or Ph.D.) in a relevant scientific discipline (pathology, cell biology, molecular biology, biomedical engineering, or related field)

7 or more years of hands-on experience in IHC/IF assay development and image analysis in a CRO, biopharma, or regulated research environment

Demonstrated experience building image analysis algorithms or pipelines in platforms such as Visiopharm, HALO, or similar

Exposure to spatial biology platforms (e.g., 10x Visium, Xenium, Akoya PhenoCycler) is a strong asset

- **Technical Skills & Competencies **:

Deep practical knowledge of chromogenic IHC and multiplex immunofluorescence, including antibody selection, panel design, optimization, and troubleshooting

Proficiency in digital pathology image analysis and quantitative biomarker readout strategies

Familiarity with AI/ML approaches for histopathology applications

Understanding of regulatory and GxP expectations for assay validation documentation

Scientific rigor and meticulous attention to detail

Ability to communicate complex scientific concepts clearly to both technical and non-technical stakeholders

Strong written and oral English communication skills; comfortable presenting at client meetings and scientific forums

Ability to manage multiple projects in a fast-paced, client-driven environment

Collaborative mindset with the ability to work across laboratory, scientific, and operational functions

Compensation is dependent on the unique experience, skills, and education the successful candidate brings to the role. The range above represents an estimated base salary that we would expect to compensate at, but we encourage applicants to speak with the member of the TA team if contacted for an initial phone screen should your expectations differ from those listed above.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

+ bonus

**Stay Alert to Recruitment Scams**

We have been made aware of individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process. Official communication will only come from our company email domains. If something doesn’t feel right, we encourage you to verify before responding.

Scientist, Computational & Digital Pathology (AcelaBio)

Revelation Pharma is a national network of 503A and 503B compounding pharmacies providing innovative and quality pharmaceutical products and services through “industry best” patient care and solutions for customers.

Compounding pharmacy will drastically change in the next five years. At Revelation Pharma, we think that this change will be most challenging yet exciting for all compounders. Talk to us and see how we view the opportunity.

Industry: Pharmaceutical Manufacturing
Company Size: 201-500 employees

Revelation Pharma

**Role Summary **

Pharmacy Technician responsibilities may include the following: compounding sterile and non-sterile pharmaceutical preparations under the supervision of the compounding pharmacist; performing fulfillment of data entry and prescription processing, and/or assisting and supporting laboratory technicians in prescription compounding and fulfillment activities. This position reports to the department team lead.

** ****Job Activities and Responsibilities: ** The responsibilities listed below are subject to change.

- Must have knowledge of and follow applicable Standard Operating Procedures and applicable state laws and regulations

- Technician shall work under the supervision of a pharmacist

- Technicians may be first point of contact for customers, so it is very important that customers are greeted and assisted in a friendly and professional manner

- Checking prescriptions for completeness and entering necessary information into the computer to generate a prescription label and invoices (if necessary)

- Filling and labeling prescriptions and prepackaging bulk medications and various types of medication and ancillary kits

- Communicating with prescribers to receive refill authorization receiving patient refills by telephone, directing calls or taking and relaying messages

- Receives patient refills and payments by telephone, directing calls or taking and relaying messages Assisting team lead with organization and appearance of the pharmacy front-end, ordering and pricing front-end merchandise.

- May also include sterile and non-sterile compounding may include but is not limited to the compounding of capsules, oral liquids, topical medications, nasal preparations, suppositories, troches, tablet triturates, lollipops, and sterile compounded products

- Investigating an incidence and/or variance as needed, documenting variances as needed including the resolution

- Other duties as determined by department team lead

** ****Qualifications and Education Requirements **

- High school diploma or equivalent

- Must be licensed by the State you are applying to work in as a Registered Pharmacy Technician

- Ability to navigate basic computer operating systems

- must have at least 3 years of pharmacy experience

- must be able to work full time immediately upon hire

**Physical Requirements: **

- Proficient in using a computer and related equipment, including printers and fax machines.

- Ability to sit or stand for extended periods.

- Effective communication skills via telephone and email.

- Capable of lifting up to 40 pounds as needed.

- 20/20 vision (with or without corrective aids) required for visual inspection of drug products, in accordance with legal requirements.

**Benefits: **

- Health care insurance (medical, dental, vision)

- Life Insurance

- Supplemental Insurance

- PTO

- 401K matching

- Sick leave

Revelation Pharma is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Pharmacy Technician

Industry: Retail
Company Size: 11-50 employees

First Glass Promotion

**Company Overview: **

PRI Construction Materials Technologies, LLC (Certerra PRI-CMT) is an independent, accredited testing laboratory dedicated to the construction materials industry; we are recognized as both an ISO/IEC Standard 17025 testing laboratory and an ISO/IEC Standard 17020 inspection agency by the International Accreditation Service, Inc. (IAS).

Our objective is simple, to provide the finest in testing, inspection, and litigation support services for our clients. Our services are backed by our state-of-the-art equipped facility, dedicated staff, and deep industry expertise. Our expertise encompasses the entire building envelope, including roof coverings, water-resistive barriers, air barriers, exterior sidings, fenestration openings, insulations & radiant barriers, ventilation systems, coatings & adhesives, and more.

In this position, you will join a team of laboratory technicians and your primary responsibility will be to complete assigned product testing. Assignments will range from benchtop physical property testing (e.g. universal tester, water vapor transmission, radiative properties, etc.) to laboratory scale mock-up performance testing (e.g. 12’ x 24’ roof assemblies for fire resistance, wind uplift resistance, 8’ x 8’ wall assemblies for water resistance performance, 4’ x 4’ floor assemblies for failure load performance, etc.). Additional responsibilities will include maintenance and calibration of test instruments, equipment, and apparatuses; interaction with clients that are on-site to witness testing; and several day-to-day administrative tasks.

Job Requirements

**Education: **

- Minimum: High School Diploma / GED

- Preferred: College Degree in Science, Engineering or Building Construction

**Experience/Skills: **

- Minimum: 1+ years of related experience (e.g. laboratory technician, construction worker, contractor, engineer, etc.)

- Preferred: 3+ years of related experience (e.g. laboratory technician, construction worker, contractor, engineer, etc.)

- Communication Skills: Minimum: Able to speak and write English fluently

- Computer Skills: Minimum: Proficient with Microsoft Office products, including MS Excel and MS Word.

- Physical Conditions: Minimum: Able to lift 50+ lbs and work in varying weather conditions, including Florida summer outside

If hired by Certerra PRI-CMT, you will join a growing business with a “can do" attitude. We offer a competitive salary and excellent benefits, including employer subsidized health/dental/life insurance, 401k retirement program with company match, and profit sharing.

Job Type: Full-time

**Benefits: **

- 401(k) matching

- Dental insurance

- Flexible spending account

- Health insurance

- Paid time off

- Vision insurance

**Schedule: **

- 8 hour shift

- Monday to Friday

- Overtime

**Work Location: ** In person

We are an Equal Opportunity Employer. This Company is dedicated to both the letter and the spirit of the equal opportunity employment laws. All applicants and all employees will be evaluated based on their ability, competence, and performance of the essential functions of their positions. There will be no discrimination based on race, sex, national origin, religion, age 40 and over, disability, sexual orientation, marital status, or any other classification which may be protected by federal, state, or local laws. In compliance with the Americans with Disabilities Act, we specifically offer equal opportunity for all employees or job applicants who may have a physical or mental disability. Such people will be hired based on their ability to perform the essential functions of the job in question. Likewise, their work will be evaluated on their performance of these essential functions. We will offer reasonable accommodation to individuals with disabilities, to the extent that Company resources allow without undue hardship. As part of our equal employment policy, there will be no wage differentials based on gender, between men and women employed in the same establishment, on jobs that require equal skill, effort, and responsibility, and which are performed under similar working conditions.

Lab Technician I-Tampa, FL

**Job Summary: **

The Senior Laboratory Technician will support laboratory operations during the third shift, performing routine and advanced analytical tasks within a manufacturing environment. This role ensures accurate testing, data integrity, and adherence to quality and safety standards. The position plays a critical role in supporting production and maintaining compliance with established procedures.

**Key Responsibilities: **

• Perform laboratory testing and analysis in accordance with established procedures and protocols

• Support manufacturing operations by providing timely and accurate test results

• Maintain laboratory equipment, including calibration, troubleshooting, and routine maintenance

• Document test results and ensure accuracy, completeness, and compliance with quality standards

• Follow standard operating procedures and maintain compliance with regulatory and safety guidelines

• Assist in identifying and resolving technical issues within the laboratory environment

• Maintain a clean, organized, and safe laboratory workspace

**Required Qualifications: **

• Associate or Bachelor’s degree in a scientific field such as Chemistry, Biology, or related discipline

• Experience working in a laboratory or manufacturing environment

• Strong understanding of laboratory practices, safety standards, and documentation requirements

• Ability to work independently during overnight shifts

• Strong attention to detail and problem-solving skills

**Preferred Qualifications: **

• Experience in analytical laboratory testing within a regulated industry

• Familiarity with quality systems and standard operating procedures in a manufacturing setting

• Prior experience working third shift in a production or laboratory environment

**Benefits: **

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.

**Pay Range: $20/hr to $25/hr **

Entry Level Laboratory Technician – Night Shift

Find Research Laboratory Technician jobs with Savvy's AI Recruiter. Browse thousands of opportunities from top companies including remote positions. Our AI-powered system matches you with roles that fit your skills and experience.