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

DataAnnotation

Savvy Admin PROD

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)

At Revvity, “impossible” is inspiration, and ""can't be done"" is a call to action. Revvity provides health science solutions, technologies, expertise and services that deliver complete workflows from discovery to development, and diagnosis to cure. Revvity is revolutionizing what’s possible in healthcare, with specialized focus areas in translational multi-omics technologies, biomarker identification, imaging, prediction, screening, detection and diagnosis, informatics and more. With more than $3 billion in revenue and over 11,000 employees, Revvity serves customers across pharmaceutical and biotech, diagnostic labs, academia and governments. It is part of the S&P 500 index and has customers in more than 190 countries. Learn more at www.revvity.com

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

Revvity

**This position is onsite in Boston until the office relocates to Hopkinton, MA in August 2026.**

**Core Duties and Responsibilities:**

Perform analyses by HPLC and labeling, dispensing and packaging of radiolabeled products (14C/3H) according to established procedures.

Conduct preparative HPLC experiments to support custom synthesis products.

Support general lab functions, setup, calibration and maintenance of equipment.

Author protocols, technical reports and SOP’s

Maintain and revise analytical protocols as necessary

Work safely and in compliance with all applicable company, federal and local regulations.

Perform transactions using ERP systems.

Participation in inventory receipt/warehousing and control of raw materials reagents, product and lab supplies.

~~Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities of this job at any time.~~

**Basic Qualifications:**

-  Bachelor's degree in life or natural sciences and 2+ years of lab experience

OR

-  Master's degree in life or natural sciences

**Preferred Qualifications:**

More than six months’ experience using HPLC is required to work independently, doing HPLC analyses.

Should have good familiarity with applicable modern analytical tools that may include HPLC, TLC, GC, KF, NMR, UV-Vis or similarly related equipment.

A good understanding of analytical chemistry, synthetic chemistry, biology or related scientific discipline.

Demonstrates application of specialized professional knowledge and skill.

Performing tasks following cGMP guidelines preferred.

**Physical Requirements:**

-  Positions may require the ability to lift 25 pounds and stand for long periods of time.

**Compensation Range:**

The annual base salary range for this full-time position is $65,500 - 87,500. This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.

**What do we offer?**

We provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits:

- Medical, Dental, and Vision Insurance Options

- Life and Disability Insurance

- Paid Time-Off

- Parental Benefits

- Compassionate Care Leave

- 401k with Company Match

- Employee Stock Purchase Plan

Learn more about Revvity’s benefits by visiting our Bswift page. Log-In instructions are provided towards the bottom of the Bswift page.

~~For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information.~~

Process Development Chemist

Kodak is a leading global manufacturer focused on commercial print and advanced materials & chemicals. With 31,000 patents earned over 130 years of R&D, we believe in the power of technology and science to enhance what the world sees and creates. Our innovative, award-winning products, combined with our customer-first approach, make us the partner of choice for commercial printers worldwide. Kodak is committed to environmental stewardship, including industry leadership in developing sustainable solutions for print.

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

Eastman Kodak Company

Kodak is looking for a Senior Chemical Operator to work in our Specialty Chemical Division (SCID) Small Scale manufacturing department. This operator will synthesize various chemicals using traditional chemistry glassware (1L to 72L) and other chemical processing equipment while maximizing output, maintaining product quality, minimizing waste, and following all safety guidelines and manufacturing procedures.

**Specialized Skills and Job Expectations: **

• Synthesize chemicals using Small Scale manufacturing equipment at 1L to 72L size.

• Strict adherence to division operation and HSE procedures.

• Follow process procedures to run reactions from starting materials through synthesis of final products.

• Plan workday to manage processes that may take hours or multiple days. Responsible for numerous types of unit operations.

• Work with area Process/Development Chemists to resolve any quality or yield issues.

• Participate in process quality/life guards as needed.

• Participate in process safety reviews and process hazard analyses as needed.

• Individual should have good interpersonal skills and the ability to work in a small team-oriented environment.

• Good communication skills are needed, both written and verbal, with the ability to express oneself clearly, read job related material, and write effectively.

• Basic computer skills including Microsoft Office and Lotus Notes.

• Individual must be able to perform basic math functions.

• Position requires working in walk-in fume hoods, standing, frequent lifting, carrying, pulling, pushing, etc.

• Individual should have good analytical and trouble shooting skills.

• Monday – Friday, 8 hour work schedule.

• Willing to work overtime or adjust work schedule for shutdowns and business needs.

**Desired Skills/Experience: **

• 10+ years of chemical manufacturing experience, mechanically inclined, and chemical/technical experience.

• Associates degree in chemistry/chemical technology or related field with 5+ years of experience will be considered.

• Good interpretation of procedures and adherence to HSE and process procedures.

• Understanding of continuous improvement and Lean Six Sigma techniques.

Senior Chemical Operator

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

**Company Description**

**About Syngenta**

At Syngenta Crop Protection, we're pioneering solutions that safeguard global food security while championing sustainable agriculture. As a world market leader headquartered in Switzerland, we empower farmers with innovative crop protection technologies that defend against nature's toughest challenges. We unite advanced science with digital solutions to develop intelligent crop protection that maximizes yields while minimizing environmental impact. Join our mission of revolutionizing plant protection from seed to harvest.

**Job Description**

At Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success. To support this mission, Syngenta's Research Chemistry Team is seeking an Analytical Scientist in Greensboro, NC. This role will support Product Chemistry Formulation (PCF) projects to enable product registrations in countries outside of North America.

The Analytical Scientist will perform a wide variety of physical properties analyses (e.g. wet chemistry) on chemical pesticides and biological pesticides, using internationally recognized physical test methods (e.g. CIPAC, ASTM, etc.). This role also includes chromatographic analyses for active ingredient content (gas chromatography and high-performance liquid chromatography).

The successful candidate will be responsible for generating fully GLP (Good Laboratory Practice) compliant raw data, protocols and reports, for submission to regulatory authorities as part of new product development projects, regulatory data call-ins, etc. This role is expected to work independently on daily tasks, while contributing to the delivery of each project as part of a highly collaborative team environment.

**Accountabilities**

- Perform physical properties testing and active ingredient content analysis of formulated products accurately, with minimal supervision.

- Strictly adhere to GLP (Good Laboratory Practice) regulatory standards independently, throughout all lab related activities.

- Develop expertise in a wide variety of internationally recognized analytical methods (e.g. CIPAC methods, etc.), strictly adhering to these methodologies.

- Organize raw data into GLP compliant raw data packets / dossiers and generate high-quality study reports.

- Develop proficiency with computer/software platforms such as Microsoft Office software, Chromeleon chromatography software, StarLims, and various other internal platforms.

- Ensure effective problem solving and independent follow-up when unexpected situations arise during testing (e.g. unanticipated test results, etc.).

- Provide consistent, proactive and effective communication within the team, with project stakeholders, data requestors, etc.

**Qualifications**

**Required:**

- Bachelor's degree in Chemistry or another related field is required.

- A minimum of 1-3 years' laboratory experience is required with a Bachelor's degree in Chemistry or other related field.

- Chromatography experience (i.e. HPLC and GC) is preferred.

- Physical properties testing experience (i.e. wet chemistry) is preferred.

- Deliver high quality analytical data on-time, data interpretation and problem solving for product development projects.

- Ability to communicate effectively and efficiently with department members, internal regulatory customers, and project stakeholders to present data, outline challenges and propose solutions.

- Ability to critically inspect and proofread their own data and documents, and those of their colleagues, to proactively find and correct any issues.

- Multi-tasking is required, as activities and testing can vary from day-to-day, depending on project scope.

**Desired**

- Maintain meticulous attention to detail and accurate recordkeeping.

- Demonstrate strong organizational skills and the ability to manage multiple priorities.

- Communicate clearly and professionally in both written and verbal formats.

- Adapt quickly to new tasks and changing priorities, as business needs require.

- Resolve issues proactively by identifying challenges early and implementing timely solutions.

- Execute assigned work independently while collaborating effectively within a flexible, team-based environment.

- Train and guide contractor work activities, as needed, to support project execution.

**Additional Information**

**What We Offer:**

- A culture that celebrates belonging and collaboration, promotes professional development and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs.

- Full Benefit Package (Medical, Dental & Vision) that starts your first day.

- 401k plan with company match, Profit Sharing & Retirement Savings Contribution.

- Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits.

Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: https://www.youtube.com/watch?v=OVCN_51GbNI

Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

**WL: 3B**

Analytical Scientist

A global leader in applied safety science, UL Solutions transforms safety, security, and sustainability challenges into opportunities for customers in more than 100 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. 

The UL Certification Marks serve as a recognized symbol of trust in our customers’ products and reflect an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. 

We believe in the possibility and promise of innovation, and we have spent more than a century enabling it to be safely adopted. From the adoption of electrification to the enablement of 5G and new mobility, we collectively look toward new frontiers, working for a safer world. Our science is your advantage.

Industry: Professional Services
Company Size: 10,001+ employees

UL Solutions

**Job Description**

UL Solutions is a global leader in safety science, providing the expertise and services organizations need to tackle critical business challenges. We help customers meet their safety, security and sustainability goals, manage risk, achieve regulatory compliance and deliver products that meet quality expectations. A Laboratory Chemist will take a hands-on approach in our testing process at our headquarters in Northbrook, IL.

**Responsibilities**

-  Follows defined test plans and datasheets with necessary supervision/support. Evaluates test performance and

sample operation to properly evaluate test results. Records and explains test results and completes test report.

-  Serves as Lead for simple test programs as assigned with the necessary assistance. Communicates project status

and results as needed. Holds responsibility for defining test plan, report completion and accuracy, meeting of agreed

deadlines, and managing project related activities.

-  Examines customer samples and learns to operate appropriate tests for each case with support. Communicates with

internal customers during setup and operation to ensure proper evaluation.

-  Directs, builds and/or adapts simple test setups, sample preparations/solutions and instruments to new situations,

based on test plans and instructions. Trains other lab staff on these test procedures or instruments.

-  Operates and maintains test instruments appropriately to measure and test samples. Performs maintenance on

designated test instruments and laboratory area.

-  For a single testing technology, integrates basic process and instruments improvements into all aspects of the job.

Communicates with management and technical staff to provide suggestions for new instruments, processes, and

forms to improve accuracy and efficiencies.

-  Understands and follows safe chemical hygiene practices.

-  Read and follow the Underwriters Laboratories Code of Conduct, and follow all physical and digital security practices.

-  Other duties as assigned

**Qualifications**

-  Bachelor’s degree or diploma from an accredited university through a formal program of study in Chemistry or related

discipline including Chemical Engineering, Biochemistry, Organic/Inorganic Chemistry, Material Science but not limited

to these disciplines only.

-  Demonstrated ability to manage multiple projects while maintaining high quality and exceptional customer service.

-  Demonstrated ability to successfully partner with Engineering and other Laboratory Personnel to complete projects in

a timely manner with high quality.

-  Demonstrated ability to analyze special testing needs.

-  Effective communication skills and ability to interact with customers

-  Demonstrated ability to be innovative and creative

-  Desire to work in a team-oriented environment

-  Ability to use Microsoft Office suite is a must

-  Ability to incorporate automation into day-to-day testing

**Total Rewards: ** We understand compensation is an important factor as you consider the next step in your career . The estimated salary range for this position is $52,900 to $70,500 and is based on multiple factors, including job-related knowledge/skills, experience, geographical location, as well as other factors. This position is eligible for annual bonus compensation with a target payout of 5% of the base salary. This position also provides health benefits such as medical, dental and vision; wellness benefits such as mental and financial health; and retirement savings (401K) commensurate with the standard rewards offered in each individual location or country. We also provide full-time employees with paid time off including vacation (15 days), holiday including floating holidays (12 days) and sick time off (72 hours).

**About Us**

A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers’ products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.

**About The Team**

Our global network of 80+ laboratories is constantly evolving, because the world around us is always changing. We embrace this — we invest in improving our equipment and our skills so we’re one step ahead of the market. One day we could be setting up a burn test and the next, simulating a tornado. And because we’re always evolving, your career will evolve alongside us, whether you’re working on brand new technology or connecting with experts around the globe. Join our team, drive the growth of our organization and deliver real change — in a changing world.

Laboratory Chemist

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

Founded in 2012, Planet Pharma is a global leader in life sciences recruitment and staffing, specializing in Pharmaceuticals, Biotechnology, Medical Device, Labs & Healthcare, Specialty Providers, CMOs / CDMOs, and Contract Research Organizations (CROs). We provide the following solutions: Contract & Direct Hire (Permanent) Staffing, Strategic Resourcing, Retained & Executive Search, Functional Service Provider (FSP), and Global Workforce Solutions.

Planet Pharma has offices throughout North America, Europe, and APAC. All locations operate with shared attributes at the heart of everything we do!

🚨 Job Scam Warning 🚨
We’ve recently been made aware of fraudulent activity where individuals are posing as representatives of Planet Pharma and contacting job seekers using fake email addresses.

✅ All genuine emails from Planet Pharma will always come from an address ending in @planet-pharma.com, @planet-pharma.co.uk, or @ppgadvisorypartners.com.

❌ We will never contact you from free email services or unfamiliar domains.

If you receive a message claiming to be from us and are unsure if it’s legitimate, reach out to us directly at contactus@planet-pharma.com for verification. Your safety and trust are our priority!

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

Planet Pharma

**Scientist II **

**Location: ** Irvine, CA (on‑site)

**Contract: ** 12 months

**Pay Rate: ** Target $45–46/hr

**Position Overview **

We are seeking a Formulation Scientist to support the development of sterile liquid pharmaceutical drug products. The ideal candidate will have hands‑on experience with liquid dosage form formulation and process development, strong laboratory execution skills, and the ability to independently generate and interpret scientifically sound data.

This role focuses on solutions, emulsions, and suspensions, with exposure to polymer science, sterilization techniques, and analytical characterization methods.

**Key Responsibilities **

- Conduct laboratory experiments supporting the development of sterile liquid dosage forms under general supervision.

- Execute analytical and characterization testing to support formulation and manufacturing process development.

- Independently design, plan, and interpret experiments as needed.

- Utilize problem‑solving and scientific reasoning to address formulation and process challenges.

- Accurately document experiments, results, and conclusions in electronic laboratory notebooks (ELN).

- Analyze and interpret technical data using fundamental statistical tools when appropriate.

- Prepare clear and concise technical summaries and reports.

- Maintain laboratory equipment and instrumentation to ensure operational readiness.

- Collaborate effectively with cross‑functional team members and communicate results clearly (written and verbal).

**Required Skills & Experience **

- Working knowledge of formulation and manufacturing process development for sterile liquid drug products, including solutions, emulsions, and suspensions.

- Experience with analytical and characterization techniques, such as:

- pH

- Osmolality

- Viscosity / Rheology

- Turbidity

- Particle size

- Physical appearance evaluations

- Knowledge of polymer sciences (highly desired).

- Familiarity with sterilization techniques for liquid drug products (e.g., filtration, autoclaving).

- Strong technical writing, documentation, and data analysis skills.

- Proficiency with Microsoft Word, Excel, and statistical software.

**Nice to Have: **

- Hands‑on experience with HPLC or UPLC (UV, PDA, RI detectors).

**Education & Qualifications **

- Bachelor’s degree in Chemistry, Chemical Engineering, Pharmacy, or related scientific discipline

- plus 3–5 years of relevant industry experience

- OR

- Master’s degree in a similar discipline

- plus 2 years of relevant industry experience

Scientist

SBA, Veteran Owned company Geater Machining and Manufacturing, Co. (Geater) has been servicing the aerospace, electronic, and high-tech industries since 1962. Our high quality parts and outstanding on-time delivery have developed Geater’s reputation into one that is synonymous with trust, and setting high standards for precision machined and fabricated parts.

Located in America's Heartland we can serve your quality and delivery needs with an award winning workforce and easy access to major interstates. 

We are a team of problems solvers committed to continuous improvement every day.  Geater's team will work with your team to provide the best quality and delivery at competitive prices.

Industry: Aviation and Aerospace Component Manufacturing
Company Size: 201-500 employees

Geater Machining and Manufacturing, Co.

**Position Summary**

The Chemical Process Engineer is responsible for designing, implementing, commissioning, and optimizing plating processes and production lines. This role leads the startup of new plating lines, ensures process stability, maintains chemical performance, and drives continuous improvement in quality, safety, and environmental compliance.

**Essential Duties and Responsibilities **include the following. Other duties may be assigned.

- Lead the installations, setup, and commissioning of new plating lines

- Develop process parameters and operating procedures

- Develop and optimize plating processes

- Manage chemical inventory procedures

- Implement root cause analysis and corrective actions

- Ensure compliance with OSHA, EPA, NADCAP, and local environmental regulations

- Oversee wastewater treatment and chemical handling procedures

- Develop standard operating procedures for plating processes

**Qualifications**

To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

- Read, write and speak English fluently, demonstrate excellent oral and written communication skills, and maintain a positive attitude and willingness to learn.

- Strong project management skills

- Ability to work with cross-functional teams

- Ability to train operators and technicians

- Knowledge of plating processes

**Education And/or Experience**

- High School Diploma, GED or equivalent work experience

- Preferred Bachelor's degree in Chemical Engineering, Chemistry, or related field

- 3-7 years' experience in plating or metal finishing processes

- Experience with plating line startup or new process implementation preferred

**Physical Demands Include**

- Sitting, standing, and walking.

- Use of fingers, hands and arms to operate office equipment.

- Being able to see (20/25 vision with or without glasses) and hear (with mechanical assistance if necessary) sufficient to understand and comprehend individual one-on-one conversations.

**Work Environment**

This person will work in the office area; temperature controlled environment with moderate noise. Often he or she will spend a significant amount of time out in the plant working with operators. The plant setting involves manufacturing equipment with others working in close proximity.

**Supervisory Responsibilities**

None

**PPE Requirements**

- Safety glasses or side shields

- Close-toed or steel-toed shoes/boots

**Job Posted by ApplicantPro **

Chemical Process Engineer

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