About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. 

For more information, please visit www.thermofisher.com.

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

Thermo Fisher Scientific

Savvy Admin PROD

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Laboratory Setting

Are you passionate about new ideas and breakthroughs? Thermo Fisher Scientific invests over $1 billion in R&D each year. Join us in solving challenging global problems, such as cancer treatment, clean drinking water, and forensic investigations. We support our colleagues in translating science into impactful solutions, providing autonomy, resources, and tools.

The Scientist III, Molecular Biology is responsible for leading technical exploration and finding effective solutions for improving molecular diagnostic products in transplant medicine. This role requires self-motivation and the ability to connect individual tasks to larger goals.

**Location **: 100% on-site West Hills, CA. Relocation assistance is NOT provided.

**Responsibilities:**

- Assist in crafting and completing feasibility studies to explore novel ideas

- Design and execute experiments following GMP practices

- Validate and record newly developed processes and protocols.

- Responsible for understanding and performing daily testing of reagents for extent, improvement, and troubleshooting HLA gene typing products or related issues.

- Handle and maintain laboratory environment and equipment needed to carry out assigned projects.

- Prepare SOPs, study plans, reports, and other internal documents as well as maintain/update current SOPs for existing products.

- Actively participate in meetings and technical problem solving

- Assist in project planning, supervise the progress, prepare and present summary reports

- Function as a lead for time-sensitive projects and provide support to the team to achieve the best results

- Conduct literature search, proactively monitor relevant diagnostic market, proactively seek opportunities for innovation, and write proposals for grants or manuscripts for publication

**Accountability:**

- Maintain confidentiality of critical laboratory and business data.

- Understand and follow Thermo Fisher quality policies and procedures

**Education/Training Experience:**

- Applicants must have Bachelors in Biological Sciences, Molecular Bio or a related field AND 5+ years of laboratory experience in an academic or R&D industrial environment. OR Master's in Biological Sciences, Molecular Bio or a related field AND 3+ years relevant post-graduate experience. OR PhD degree in Biological Sciences, Molecular Bio or a related field with a minimum of 1 year of relevant post-doctoral experience.

**Knowledge, Skills, Abilities:**

- Knowledge of molecular biology and recombinant DNA techniques

- Strong understanding of molecular biology and relevant techniques such as DNA isolation and quantification, gene amplification methods, quantitative PCR, sequencing, and other relevant technologies

- Experience with primer and probe designs

-  Experience in crafting experiments and interpreting data and addressing issues to improve product performance with innovative solutions.

- Ability to collaborate with diverse groups of people, strong communication skills

- Ability to support process improvement, customer inquiries, staff training as needed

- Well-developed written communication abilities, experience in preparing technical documentation such as plans, reports, technical reviews. Ability to prepare technical publications and presentations

- Must be legally authorized to work in the United States without sponsorship.

- Must be able to pass a comprehensive background check, which includes a drug screening.

**Compensation And Benefits**

The salary range estimated for this position based in California is $91,700.00–$137,525.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Scientist III Molecular Biology R&D (West Hills, CA)

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Laboratory Setting

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

**Location:**

This is an onsite position in Bedford, MA. Residency near the site is required, no relocation assistance provided.

DESCRIPTION:

Join our team at Thermo Fisher Scientific as a Manufacturing Sciences Scientist III, where you'll contribute to global health through innovative process development and optimization. You'll provide technical leadership in technology transfer, process validation, and manufacturing support across our facilities. Working at the intersection of R&D and manufacturing, you'll collaborate with cross-functional teams to ensure successful execution of manufacturing processes while driving continuous improvement initiatives. Your expertise will be vital in resolving complex technical challenges, conducting investigations, and implementing solutions that maintain our high standards of quality and efficiency.

REQUIREMENTS:

-  Advanced Degree plus 5 years of experience, or Bachelor's Degree plus 8 years of experience in GMP-regulated pharmaceutical/biotech manufacturing

-  Preferred Fields of Study: Chemistry, Biochemistry, Biotechnology, Chemical Engineering, or related scientific field

-  Strong technical expertise in process development, scale-up, and technology transfer

-  Advanced understanding of polymerization chemistry

-  Proven ability to lead complex investigations and implement effective solutions

-  Experience with process validation and qualification activities

-  Expert knowledge of cGMP regulations and quality systems

-  Strong analytical and statistical analysis capabilities

-  Advanced project management and documentation skills

-  Excellent verbal and written communication skills

-  Ability to work collaboratively in a matrix environment

-  Proficiency with statistical analysis software and Microsoft Office suite

-  Experience mentoring colleagues and providing technical training

-  Strong problem-solving skills and attention to detail

-  Ability to support manufacturing operations as needed, including occasional weekend/off-hours coverage

-  Travel between local sites up to 20% may be required

**Compensation And Benefits**

The salary range estimated for this position based in Massachusetts is $84,000.00–$111,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Manufacturing Scientist III, Chemistry (Onsite)

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

At Thermo Fisher Scientific, our mission is to enable our customers to make the world healthier, cleaner, and safer. Within the Clinical Sequencing Division, bioinformatics plays an important role in enabling precision oncology diagnostics and advancing genomic medicine.

**Location/Division-Specific Information:**

Carlsbad, CA, or Austin, TX. Relocation assistance is NOT provided.

- Must be legally authorized to work in the United States without sponsorship.

- Must be able to pass a comprehensive background check, which includes a drug screen.

**Discover Impactful Work:**

As a **Scientist III, Bioinformatics **, you will contribute to the development and maintenance of bioinformatics applications, data systems, and computational workflows that support next-generation sequencing (NGS) companion diagnostic (CDx) assay development.

In this role, you will collaborate with scientists, engineers, and cross-functional partners to develop tools and workflows that support genomic data analysis, assay development, and regulated diagnostic programs. Your work will help ensure that bioinformatics systems supporting diagnostic development are reliable, reproducible, and well-documented.

You will also contribute to emerging initiatives that explore the use of **AI-enabled tools ** to enhance bioinformatics workflows, data analysis, and internal scientific applications.

This position combines bioinformatics expertise with scientific software development to support scalable genomic analysis and integration with laboratory and data management systems.

**A Day in the Life:**

Bioinformatics Application Development

Develop and maintain internal bioinformatics applications and computational tools to support genomic data analysis and the development of companion diagnostic assays.

Workflow and Pipeline Development

Implement and improve automated workflows for next-generation sequencing (NGS) data processing and analysis using scripting languages and workflow frameworks.

Data Systems and Integration

Support development and integration of bioinformatics workflows with data systems, databases, and laboratory information management systems (LIMS).

AI-Enabled Workflow Support

Contribute to the evaluation and integration of AI-enabled tools that enhance bioinformatics workflows, scientific data analysis, and internal research applications.

Cross-Functional Collaboration and Documentation

Work with scientists, engineers, and program teams to develop computational solutions supporting diagnostic development and document workflows to ensure reproducibility and maintainability within regulated environments.

**Keys to Success**

**Education**

Bachelor’s in Bioinformatics, Computational Biology, Computer Science, Molecular Biology, or a related field required.

**Experience**

- 5 years of experience in bioinformatics and NGS data analysis (Advanced degree plus 3 years of experience).

- Experience programming in Python or a similar language.

- Experience working in Linux or Unix environments.

- Experience developing or supporting bioinformatics pipelines or analysis tools.

- Familiarity with next-generation sequencing (NGS) data analysis.

- Experience using version control systems such as Git.

- Experience collaborating with cross-functional scientific teams.

**Knowledge, Skills, And Abilities**

Programming and Scientific Computing

- Proficiency in Python or similar programming languages.

- Experience developing scripts, tools, or applications for scientific data analysis.

- Familiarity with software development practices such as version control and documentation.

Bioinformatics and Genomics

- Understanding of common bioinformatics workflows and sequencing data formats.

- Experience working with genomic datasets.

Data Systems

- Familiarity with databases or structured data systems (e.g., SQL).

- Experience working with large or complex scientific datasets.

Workflow and Infrastructure

- Familiarity with workflow frameworks such as Nextflow, Snakemake, or similar tools.

- Experience with container technologies such as Docker is helpful.

- Exposure to cloud computing platforms such as AWS or GCP is beneficial.

AI and Emerging Technologies

- Exposure to AI or machine learning tools used in scientific computing or data analysis is a plus.

- Interest in applying AI-enabled tools to improve scientific workflows.

Collaboration and Communication

- Ability to communicate technical information clearly.

- Ability to work effectively in collaborative, multidisciplinary teams.

- Strong problem-solving and analytical skills.

**Benefits:**

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

**Compensation And Benefits**

The salary range estimated for this position based in California is $95,900.00–$120,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Scientist III, Bioinformatics

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Fluctuating Temps hot/cold, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

**Discover Impactful Work**

You'll provide expert installation, maintenance, and repair services for sophisticated analytical and microscopy equipment. Working with advanced technology, you'll deliver outstanding technical support while building strong relationships with customers across research institutions, universities, and industrial facilities. You'll resolve complex issues, conduct preventive maintenance, and train users to ensure optimal system performance. This role offers excellent opportunities for professional growth and development within an organization dedicated to serving science.

**Location**

This is a remote role based in the SF Bay Area, CA and will require up to 75% travel within the designated territory and up to 25% within the West Coast. Please note that relocation assistance is not provided.

**A Day in the Life**

- Perform on-site installation, preventive maintenance, and repair support for Chromatography and Mass Spectrometry equipment at customer labs

- Handle personal parts inventories, complete job tasks and complete service reports using service ticket management software

- Train customers in equipment and software

- Provide a communication link between the customer and the company to help ensure that effective service is provided to the customer

- Regularly attend factory provided technical and service training on newest innovative products developed by Thermo Fisher Scientific

- Must be team focused while working in conjunction with Service and Sales teams

- Review customer data and run factory protocols to troubleshoot instrumentation

- Share diagnostic information with engineering, factory, field service, management, and other personnel to expedite repairs

**Keys to Success**

**Education**

Bachelor's degree in Electronics, Engineering, Physics, Chemistry, or related technical field and 5+ years of hands-on technical experience installing, troubleshooting and repairing complex analytical instruments or Advanced degree and 3+ years of experience

**Experience, Knowledge, Skills, Abilities**

- Strong diagnostic and problem-solving abilities for hardware and software issues

- Demonstrated expertise with ultra-high vacuum systems, high voltage electronics, and complex electro-mechanical systems

- Ability to read and interpret technical documentation, schematics, and engineering drawings

- Experience documenting service activities and preparing detailed reports

- Effectively train and support customers with equipment operation

- Adherence to safety protocols and quality standards

- Experience mentoring and training others preferred

- Demonstrated success in meeting customer satisfaction goals

- Excellent customer service and communication skills, both written and verbal

- Strong organizational and time management capabilities

- Strong problem-solving abilities and capacity to work independently

- Proficiency with Microsoft Office suite and service management software

- Physical ability to lift up to 50 lbs. and work in various laboratory environments

**Other**

- Must be legally authorized to work in the United States without sponsorship now or in the future

- Must be able to pass a comprehensive background check and drug screen

**Compensation And Benefits**

The hourly pay range estimated for this position based in California is $43.70–$55.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Field Service Engineer III (LCMS) SF Bay Area, CA

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

Join us as a Scientist!

This is a fully onsite role based at our customer’s site in **Collegeville, PA.**

We welcome applicants from all locations within the US.

Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

**Summarized Purpose**

Our team is searching for a Scientist who will be responsible for the analysis of biological samples using Liquid-Chromatography and Mass Spectrometry to deliver PK and PD endpoints for clinical studies across the client portfolio.

**Essential Functions:**

- Perform analysis of drugs, metabolites, and biomarkers in biological samples to applicable standards using defined analytical methods.

- Produce written analytical methods, reports, and report contributions.

- Ensure that work is performed in compliance with the relevant regulations (primarily GCP), with procedures guided by applicable government regulations, and relevant SOPs.

- Handle human biological samples and perform experimental work in accordance with HBSM, safety and data integrity guidelines.

**Education and Experience: ******

- BS in Chemistry, Biochemistry or related discipline with 2 years of related experience

- Basic knowledge and hands-on experience with LC/MS and/or quantitative bioanalytical methods.

- Understanding of regulatory requirements for GLP and GCP analytical activities.

- Excellent computer skills for communication and report writing

**In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.**

**Knowledge, Skills, and Abilities:**

- Experience with analysis and reporting of preclinical or clinical PK data.

- Experience handling of human biological samples.

- Proven experience and ability to troubleshoot methodological issues

- Experience utilizing laboratory information management systems for daily job functions.

- Highly motivated team player with a proactive attitude, excellent organizational skills and a demonstrated ability to interact effectively within a multi-disciplinary team

Working Conditions and Environment:

-  Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

-  Occasional drives to site locations, occasional domestic travel.

-  Exposure to biological fluids with potential exposure to infectious organisms.

-  Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.

-  Personal protective equipment required such as protective eyewear, garments and gloves.

-  Exposure to fluctuating and/or extreme temperatures on rare occasions.

Physical Requirements:

-  Ability to work in an upright and /or stationary position for 6-8 hours per day.

-  Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.

-  Occasional mobility needed.

-  Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

-  Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

-  Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

-  Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

-  Frequently interacts with others to obtain or relate information to diverse groups.

-  Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.

-  Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

-  Regular and consistent attendance.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Scientist, Mass Spec

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

**Location/Division Specific Information:**

This role is in the Single Use Division supporting BEA and will be located on site at either our Logan, Utah or Lebanon, Tennessee locations. Most role-related activities occur in the Santa Clara, CA area. Candidates should expect to travel approximately once a month during the initial onboarding period, with travel needs evolving based on business demands. This role is intended to operate on the first shift (day shift) Monday – Friday.

**The Sr Manager, Procurement Partner – (Division, BEA) ** contributes to the development of multi-year strategies and business plans for the Division. Leads the execution of initiatives and programs within the Division that deliver results in line with short- and long-term goal. Aligns internal and external partners and cross-functional internal teams to advance key business drivers, such as supply continuity, quality, cost and operational performance. Mitigates risk, uses technology, improves processes and systems, and reduces overall cost of ownership and acquisition

**How You Will Make an Impact:**

- Supports and promotes the internal business groups with supplier/supply chain rationale and direction

- Delivers on key objectives (Annual Operating Plan - AOP), delivery, quality, service, cost, innovation, and growth commitments for Division Procurement

- Monitors operational supplier metrics to deliver objective “Supplier Relationship

- Responsible for monthly Value Capture reports, monthly communication plan on initiatives impacting the region

- Serves as point of escalation for sites with supplier issues; manage resolution with appropriate functions

- Drives process optimization and best practices

**A Day in the Life:**

**Technical Responsibilities**

- Supports regulatory compliance activities: internal tracking systems, audit requirements, internal change controls, etc.

- Collaborates with Site to gather Category Strategy and Sourcing requirements, gain sign-off on supplier selections and awards

- Rationalizes and uses the vendor base on a category basis, measures and improves "compliance" with the corporate contracts

**Leadership Responsibilities**

- Provides strategic leadership and direction to the operational (site) procurement groups to support overall goals for performance including Right First Time (RFT), On Time in Full (OTIF), Purchase Price Variance (PPV) savings targets, and Quality Assurance

- Partners with key internal functions (e.g., COE’s ) to ensure categories strategies will be identified and implemented in accordance with COE’s Support and implement category strategy using SSMF Methodology

- Mentors and develop staff through coaching and development plans to address individual areas of improvement

- Implement talent initiatives to improve Employee Involvement Survey results

**Education:**

- A Bachelor’s degree in Supply Chain/Materials Management, Business Logistics or a related area or equivalent; MBA preferred

**Experience:**

- A minimum of 10 years of procurement / category management experience

- 3+ years’ experience of negotiation skills and formulating the business requirements for a commercial trade contract

- 3+ years’ experience of global sourcing for a global multinational manufacturing company and leading Global Value Sourcing projects, “Cradle to Grave”

- 3+ years’ experience with the usage of electronic sourcing tools for RFI, RFQ, Reverse Auction (ARIBA)

- Minimum of 5 years of progressive experience in commodity sourcing or direct project sourcing and management or purchasing and commercial management

- 3+ years' experience leading and managing procurement teams with a focus on mentoring, coaching and performance management

- Experience from a project management role under a consultancy organization or a facility manager role under a multinational company is desired

- Experience with low-cost sourcing and supplier quality assessment.

**Knowledge, Skills, Abilities:**

- Familiar with the customer bidding process and suppliers in a commercial pharma contracting industry is a strong plus

- Demonstrated success in developing and fostering relationships with suppliers while driving lower costs, superior performance and continuous improvement

- to negotiate and write supply agreements

- Excellent people skills, project management skills, good business knowledge and a teammate

- Proactive and result oriented

- Ability to work in multi-tasking and a multi-cultural environment

**Physical Requirements and Work Environment:**

- On‑site role

- Office setting

**What We Offer:**

- Annual performance-based bonus

- Annual merit performance-based increase

**Excellent Benefits:**

- Benefits & Total Rewards | Thermo Fisher Scientific

- Medical, Dental, & Vision benefits - Effective Day 1!

- Paid Time Off & Designated Paid Holidays

- Retirement Savings Plan

- Tuition Reimbursement

- Employee Referral Bonus

- Career Advancement Opportunities

Sr Manager, Procurement/Sourcing

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

**Title: Process Engineer (Fully Onsite)**

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

**Division/Site Specific Information**

You'll be based in our Florence, South Carolina location, where you'll have the opportunity to work in a dynamic environment that fosters innovation and collaboration. You will support our Drug Substance Division at Thermo Fisher Scientific and play an important role in our company's success.

**Discover Impactful Work:**

Under the direction of manager or senior engineer, assist the Engineering and Manufacturing groups to achieve site and departmental objectives. Provide technical support to support new equipment installations. Perform process simulations and assist in equipment design and optimization. Participate in cross-disciplinary project teams as necessary.

**A Day in the Life**

- Administer, document and maintain the Patheon Quality Systems conformance to regulatory requirements and company policies where appropriate through effective utilization of Patheon Quality Systems tools, as well as direct actions.

- Assist in technical aspects of the process including approving/reviewing lifecycle documents including P&IDs, criticality assessments, Quality Risk Assessments, Qualification/Validation documentation, and EH&S Process Hazards Analysis. Ensures documents are accurate and current.

- Provide technical expertise in end to end processes including facility design, materials, cleaning, planning, maintaining, producing, and shipping.

- Assist in Process and Technology Transfers.

- Maintain state-of-the-art expertise in pharmaceutical and chemical processing technology.

- Ensure regulatory compliance and drive continuous improvement in EH&S/Quality/Efficiency to improve right first time in all areas.

- Conduct technical training.

- Perform other duties as required.

- This position generally does not include supervisory responsibilities but may mentor other engineering personnel, including co-ops and interns.

**Keys to Success:**

**Education**

- Bachelor of Science in Engineering (Chemical) required.

- An advanced degree is preferred.

**Experience:**

- 3-5 years of related experience required.

**Knowledge, Skills, Abilities**

- Knowledge of regulatory requirements which includes FDA, EPA/DHEC and OSHA.

- Basic knowledge of statistical process control including Lean concepts, process and equipment modeling tools (such as ChemCAD or Aspen), business systems such as SAP, and Microsoft Office tools (including MS Project).

- Ability to prepare and interpret P&IDs, engineering drawings, engineering specifications, vendor manuals, etc.

- Excellent oral, written and presentation/communication skills; ability to interact effectively with all levels of employees; ability to multi-task and work under tight deadlines.

Physical Requirements:

While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; sit and to talk, hear or smell. The employee is occasionally required to walk and stoop, or kneel, crouch. The employee must also occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, depth perception, and ability to adjust focus.

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made for persons with disabilities -employee evaluation to determine fitness will be made by company physician(s). While performing the duties of this job, the employee is:

- Occasionally exposed to various types of chemical substances. Carcinogens, Corrosives, Irritants, Toxins, Teratogens, Mutagens, lethals (MSDS information for review on an on-going basis).

Employee must comply with all applicable safety and security procedures:

- Determine appropriate action beyond guidelines

- Report potentially unsafe conditions

- Conduct compliance monitoring, investigations and training within area of responsibility

**Benefits**

We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.

Process Engineer

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Join Thermo Fisher Scientific's Quality Assurance team and contribute to our mission to make the world healthier, cleaner and safer. As a Quality Engineer II, you will ensure compliance with quality standards and regulatory requirements across our manufacturing operations. You'll collaborate with cross-functional teams to drive continuous improvement initiatives, lead investigations, and implement corrective actions to maintain our high standards of product quality. This role offers exposure to innovative technologies and the opportunity to directly impact patient care through quality oversight of critical products.

Performs statistical analysis and works with manufacturing to investigate, conduct root cause analysis, recommend corrective actions for processes and products and to contribute to and track data to support site level performance to KPIs (e.g. yield improvements, CAPA, complaint and scrap reduction). Those activities include the planning, development and support of processes, procedures and test plans in order to ensure that products manufactured meet internal, customer and regulatory requirements

REQUIREMENTS:

-  Advanced Degree with no prior experience, or Bachelor's Degree plus 2 years of quality assurance experience in GMP/ISO regulated environments, preferably in medical devices, pharmaceuticals or biotechnology

-  Preferred Fields of Study: Life Sciences, Engineering, Chemistry or related scientific/technical field

-  ISO 13485/FDA Lead Auditor certification beneficial

-  ASQ certification (CQE, CQA) advantageous

-  Strong knowledge of quality systems, cGMP regulations, and standards including ISO 9001:2015, 21 CFR Part 820, 21 CFR Part 211

-  Expertise in quality tools and methodologies including risk management, root cause analysis, CAPA, and change control

-  Demonstrated experience leading investigations, analyzing quality data, and implementing effective corrective actions

-  Excellent documentation and technical writing skills for developing SOPs, protocols and reports

-  Strong proficiency in quality management software (TrackWise, SAP QM, etc.) and Microsoft Office suite

-  Experience conducting internal audits and supporting external regulatory inspections

-  Demonstrated ability to build consensus and collaborate across functions

-  Strong verbal and written communication skills

-  Ability to work independently while contributing effectively in team environments

-  Strong attention to detail with analytical and problem-solving capabilities

-  Experience with statistical analysis tools and quality metrics reporting

-  Project management skills and ability to prioritize effectively

-  Ability to work in clean room environments when required

-  Designee for QE Manager as required including attending meetings, participating in customer audits, represent QE team at technical visits and on customer calls.

-  Strategically planning across the network supporting AQP establishment/strengthening the QE teams as one global network teams.

-  Support the site change control system including process risk assessment in the form of FMEA tools.

-  Works directly with customers on complex critical quality issues/complaints. Leads issue/complaint resolution.

Engineer II, QA - Miami, FL

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

**Regional Sales Manager (Safety Security Solutions)**

**R-01347203**

Northeast Territory

Travel up to 75%

Come join the world leader in serving Science! As part of an outstanding team of professionals at Thermo Fisher Scientific, you’ll play an important role in helping customers make our cities and communities safer as you develop and maintain customer relationships within various state and local government agencies.

As a Regional Sales Manager (Safety Security Solutions) at Thermo Fisher Scientific, you'll support sales growth and customer success for our advanced analytical and scientific instruments. Within Thermo Fisher Scientific’s Chemical Analysis Division, you will have a real-world impact by leading all aspects of the sales process for our handheld, Field & Safety Instruments using portable molecular spectroscopy (Raman & FTIR) techniques for unknown chemical identification. As an Instrument Sales Representative, you’ll develop effective customer relations and create opportunities with state agencies and local law enforcement markets to achieve sales goals.

**What We Do**

- Schedule and coordinate in-person meetings with state or local government customers within the sales region.

- Provide presentations and demonstrations of our technology to existing and prospective customers.

- Identify new business opportunities in law enforcement, fire hazmat and narcotics identification markets.

- Work with channel partners including forecasting, training and goal setting

- Provide input in technical consultation and problem solving to meet customer needs.

- Meet or exceed established sales goals by delivering bookings commitments in accordance with business unit targets.

- Build and implement strategies and tactical plans to drive growth.

- Communicate bookings outlook to management and the broader organization to ensure transparency into performance and timely delivery of products and services.

- Drive collaboration and accountability through improved sales pipeline and forecast management processes by using sales tools like Salesforce.com.

- Work with product management teams and make recommendations based on the understanding of marketing and new product plans.

- Prepare quotations and tender submissions for the market area in liaison with management and carry out follow-up with customers for products and services.

- Participate in trade shows and technical seminars/workshops

**Education:**

- Bachelor’s degree in chemistry or related sciences preferred.

**Experience:**

- Commercial experience selling to public safety customers (law enforcement, fire hazmat)

- Technical knowledge of analytical instrumentation and applications

- Experience with CRM systems (e.g., Salesforce.com) and MS Office suite

**Knowledge, Skills, Abilities:**

- Effective consultative selling and negotiation skills

- Ability to develop and execute strategic sales plans

- Strong presentation and communication skills

- Project management and organizational abilities

- Ability to build and maintain relationships with customers and internal stakeholders

- Experience working in collaborative environments

- Fluency in English required, additional languages beneficial

- Valid driver's license and ability to travel up to 75%

- Resides within the primary sales territory (Northeast U.S. near major airport).

- Commitment to Thermo Fisher Scientific's values of Integrity, Intensity, Innovation and Involvement

The base salary range estimated for this position based in Massachusetts is $71,300.00–$107,000.00. This position may is also be eligible to receive a variable annual bonus monthly commission based on company, team, and/or individual performance results in accordance with company policy. Total compensation including base salary and commission at plan would be $123K - $177K. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

**Compensation And Benefits**

The salary range estimated for this position based in Massachusetts is $71,300.00–$107,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Regional Sales Manager (Safety Security Solutions)

**Work Schedule**

**Other**

**Environmental Conditions**

Office

As part of our PPD clinical research team, you’ll have the opportunity to support groundbreaking studies that make a real difference in patients’ lives.

Position Summary

As a Customer Assistance Specialist, you will provides high quality customer service to client customers including consumers, health care professionals (HCPs), and client personnel. Documents interactions according to PPD and client guidelines. Identifies adverse events (AEs) and product complaints (PCs). Processes fulfillment (e.g., mail, fax, e-mail) and performs administrative responsibilities as needed.

What You'll Do:

- Provide high quality customer service to client customers including consumers, HCPs, and client personnel.

- Document interactions according to PPD and client guidelines. Identifies AEs events and PCs.

- Maintain knowledge of policies and procedures including client products, SOPs, protocols, GCPs, and all applicable regulatory requirements.

- Process medical information request (e.g., fulfillment) via e-mail; fax and regular mail.

- Perform line checks and system verifications, and generate reports.

- Perform other duties as assigned.

Rquired Education and Experience:

-  High School diploma / Secondary school diploma or equivalent and relevant formal academic / vocational qualification

-  Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to

at least 2 years) or equivalent combination of education, training, & experience

-  In some cases a second language may be required

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Working Enviornment:

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

- Work is performed in an office environment with exposure to electrical office equipment

- Constant interaction with clients/associates required

- Constant attention to detail-visual, mental

- Constant multi-tasking

- Daily exposure to high pressure, intense concentration needed

- Rotating shifts may be required

- Occassional driving to site locations with occasional travel

- Frequently stationary for 4-6 hours per day

- Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists

- Occasional mobility required

- Occasional crouching, stooping, bending and twisting of upper body and neck.

- Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. or 6-9 kgs.

- Ability to access and use a variety of computer software developed both in-house and off-the-shelf

- Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences

- May interact with others, relating and gathering sensitive information. Interaction includes diverse groups

-  Works with guidance or reliance on oral or written instructions from management. May require periods of intense concentration

-  Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence

-  Regular and consistent attendance

Medical Communications Customer Assistance Specialist

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

At Thermo Fisher Scientific, you’ll do meaningful work that makes a global impact—helping customers make the world healthier, cleaner, and safer. Join a collaborative, high-performing organization where innovation, speed, and customer focus drive everything we do.

As a Senior Sales Manager, you will lead and develop a high-performing commercial team in a fast-paced, dynamic environment. You will be responsible for driving strategic growth across the Single Use Technologies portfolio—including bioprocess containers, rigid systems, and hardware/consumables—while building a culture of accountability, agility, and continuous improvement.

This role requires a hands-on leader who can coach and inspire sales professionals, navigate complex markets, and execute with urgency to capture new opportunities and expand market share.

**Location:**

This is a remote Leadership position covering a North America Territory. Residency within the USA is required, preference for residency on EST or CST timezones. No relocation assistance will be provided.

**What You’ll Do:**

- Lead, coach, and develop a team of sales professionals to achieve and exceed revenue targets

- Drive territory and regional strategy, focusing on pipeline generation, opportunity conversion, and market expansion

- Foster a high-energy, performance-driven team culture in a rapidly evolving commercial environment

- Partner cross-functionally with Product Management, Marketing, Account Managers, and Field Applications to deliver customer-focused solutions

- Leverage market insights, competitive intelligence, and data analytics to inform strategy and decision-making

- Support new product launches and strategic initiatives to accelerate growth

- Build strong relationships with key customers and stakeholders across biotech, pharma, and research markets

- Utilize CRM tools (Salesforce) to manage pipeline, forecast accurately, and drive operational excellence

**What You Bring:**

- Bachelor’s degree in Life Sciences, Engineering, Business, or related field

- 7+ years of sales experience, with 2+ years of leadership or team management experience preferred

- Strong understanding of bioproduction, life sciences, or related markets required

- Proven success in driving revenue growth and leading teams in a high-paced, dynamic sales environment

- Demonstrated ability to coach, develop, and motivate high-performing teams

- Strategic mindset with strong analytical and problem-solving skills

- Excellent communication, negotiation, and stakeholder management abilities

- Experience with CRM systems (Salesforce preferred) and data-driven sales management

- Ability to travel (~40–60%) to support team and customer engagement

This is an opportunity to step into a critical leadership role where you’ll shape team performance, drive commercial success, and contribute to advancing life-changing science.

**Compensation And Benefits**

The salary range estimated for this position based in Massachusetts is $144,000.00–$190,100.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Sr. Technical Sales Manager, Single Use Technologies (North America)

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

Role: Scientist, Formulations

This is a fully onsite role based at our customer’s site in Collegeville, PA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to demonstrate the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

As a Scientist supporting the Pharm Dev Steriles in our client's Pharmaceutical R&D, you will have the opportunity to apply technical skills and expertise to develop drug product formulations and associated manufacturing processes as part of a matrix technical team. You will also use creative thinking to drive drug development of a variety of sterile product dosage forms

**Key Responsibilities:**

- Completes pre-formulation, formulation and process development activities based on established protocols and procedures

- Assists in the manufacture of batches of product as required, e.g. for process development, stability studies or clinical trials

- Coordinates activities within Pharmaceutical Development and with analytical and manufacturing representatives to meet project results

- Works with the team to align and implement pre-formulation, formulation and process development activities including authoring or contributing to manufacturing batch records

- Identify and begin to interpret any problems in the execution of experimental processes and/or in results and communicates them to supervisor

- Proactively engage and seek assistance from other scientists to solve problems

- Maintains cleanliness in own work area and in communal work areas

- Anticipates/recognizes potential problems with equipment and/or supplies, and proposes/initiates action to solve or prevent problems

- Operates equipment for which is trained independently with due regard for GMP and Safety

- Demonstrates timely & reliable recording of laboratory data in Labware and other suitable systems in accordance with company policy and legal requirements.

- Performs data management tasks including recording results successfully and in compliance with departmental guidelines in a laboratory notebook or computer (e.g. tabulating and graphing results)

- Consults with supervisor when difficulties arise that cannot be readily resolved

- Prepares oral or written summaries of results with interpretation for project work

- Writes specific technical sections of internal and external reports with supervision

- Attends regular safety training and is fully aware of safety requirements for their laboratory/working environment

- Maintains accurate and complete safety records consistent with company policy and legal requirements

- Recognizes potential safety problems and takes action to resolve them

**Basic Requirements:**

- BS degree with 2-4 years of experience in an appropriate subject area

- Is technically proficient in a number of formulation/process development techniques.

- Has good knowledge of GMP and GLP requirements, SOPs and policies

- Has operational knowledge of routine laboratory/plant equipment

~~In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.~~

Working Conditions and Environment:

-  Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

-  Occasional drives to site locations, occasional domestic travel.

-  Exposure to biological fluids with potential exposure to infectious organisms.

-  Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.

-  Personal protective equipment required such as protective eyewear, garments and gloves.

-  Exposure to fluctuating and/or extreme temperatures on rare occasions.

Physical Requirements:

-  Ability to work in an upright and /or stationary position for 6-8 hours per day.

-  Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.

-  Occasional mobility needed.

-  Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

-  Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

-  Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

-  Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

-  Frequently interacts with others to obtain or relate information to diverse groups.

-  Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.

-  Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

-  Regular and consistent attendance.

**Benefits:**

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued

Scientist, Formulations

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Able to lift 40 lbs. without assistance

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

**Location**

This is a remote role based in the New Jersey/New York territory, including Long Island, and will require 50–75% travel within the designated area. Relocation assistance is not provided.

**Discover Impactful Work**

As a Field Service Engineer II at Thermo Fisher Scientific, you'll contribute to delivering excellent service for sophisticated analytical and scientific instruments. Working with customers across research, industrial, and healthcare settings, you'll install, maintain, troubleshoot, and repair complex equipment while providing exceptional customer service. This position offers opportunities to work with advanced technology while contributing to scientific advancement and innovation.

**A Day in the Life**

- Perform installation, preventive maintenance, troubleshooting, and repair of Trace Elemental Analysis instruments, including ICP-MS, AAS, and related systems, at customer sites.

- Diagnose electronics, mechanical, ultra-high vacuum, high-voltage, and system-level issues to restore instrument performance.

- Provide responsive, professional customer support while meeting service commitments and customer satisfaction goals.

- Train and support customers on equipment operation, maintenance practices, and basic troubleshooting.

- Accurately document field service activities, including installation report and service work report, and submit timely through the required system

- Assist Commercial Teams with technical information, training, and demonstrations

- Manage territory activities effectively, including scheduling, travel planning, parts coordination, and timely communication with customers and internal teams.

- Partner with internal technical support, service leadership, and cross-functional teams to resolve complex customer issues.

**Keys to Success**

**Education**

- Bachelor's Degree in Electronics, Engineering, Physics, Chemistry, or a related technical field with 2+ years of hands-on technical experience installing, troubleshooting, and repairing complex analytical instruments or Advanced Degree with no prior experience required

- Additional relevant certifications are advantageous

**Experience**

- Hands-on technical experience installing, troubleshooting, and repairing complex analytical, scientific, laboratory, or related technical equipment.

- Experience documenting service activities, preparing detailed reports, and using service management software.

- Demonstrated success meeting customer satisfaction goals and supporting customers in technical environments.

**Knowledge, Skills, Abilities**

- Strong electronics and mechanical troubleshooting skills, with the ability to diagnose issues down to the component level.

- Ability to read and interpret technical documentation and schematics.

- Ability to effectively train and support customers on equipment operation.

- Excellent customer service and communication skills, both written and verbal.

- Strong organizational and time management capabilities, with the ability to work independently in a field-based environment.

- Strong problem-solving abilities and the ability to prioritize customer needs in a fast-paced service environment.

- Proficiency with Microsoft Office suite and service management software.

- Physical ability to lift up to 50 lbs. and work in various laboratory environments.

**Other**

- Must be legally authorized to work in the United States without sponsorship now or in the future.

- Must be able to pass a comprehensive background check and drug screen.

- Valid driver's license.

**Compensation And Benefits**

The hourly pay range estimated for this position based in New Jersey is $31.73–$42.31.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Field Service Engineer (TEA) – NY/NJ

**Work Schedule**

Standard Office Hours (40/wk)

**Environmental Conditions**

Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Join our team as a Manufacturing Sciences Scientist II, where you'll contribute to ensuring consistent production of therapeutic and diagnostic products. As part of our Manufacturing Sciences team, you'll work at the intersection of research and production, supporting process optimization, technology transfer, and continuous improvement initiatives. You'll collaborate with cross-functional teams to resolve technical challenges and ensure robust, scalable manufacturing processes that meet quality standards.

As a Manufacturing Scientist II, you will lead and/or implement activities for the development of new and established manufacturing processes of solids, liquids, and semi-solid dosage forms. Project management skills will be applied to implement the scaling up manufacturing processes, supporting new product validations and post approval qualifications activities. This will require the writing, approval, and routing documents within a manufacturing setting.

You will be the primary technical representative on client projects and will work closely work with internal and external project teams of analytical, quality, and project management representatives. Supporting process development and commercial activities will be required. Leads technical/scientific project activities and discussions to lead strategies and technical solutions that meet client needs and expectations.

Investigates, creates, and validates new scientific and equipment methodologies for a diverse scope of projects. Using experimental design, established formulation processes for the following phases of product scale-up, registration, and validation.

Creates processes and equipment design for clinical, scale up, and/or registration batches, including technology transfer of projects to and from clients. Leads problem solving activities as necessary with independent judgement. Makes decisions that require choosing between multiple options or may develop new options to resolve moderately complex problems.

REQUIREMENTS:

-  Advanced Degree with no prior experience required, OR Bachelor's Degree plus 2 years of experience in GMP manufacturing, process development, or related technical role

-  Preferred Fields of Study: Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or other related science or technical field is required.

-  Strong understanding of cGMP requirements, regulatory compliance, and quality systems

-  Experience with process validation, technology transfer, and scale-up activities

-  Strong project management and documentation skills

-  Excellent written and verbal communication abilities

-  Ability to work independently and collaboratively in a dynamic environment

-  Demonstrated problem-solving and troubleshooting capabilities

-  Proficient with Microsoft Office Suite and relevant manufacturing/quality systems

-  Experience with risk assessment and root cause analysis

-  Ability to train and support team members

-  May require occasional weekend/off-hours support

-  Must be able to wear required PPE and work in controlled environments

-  Physical requirements include ability to lift up to 35 lbs and stand for extended periods

-  Additional language skills beneficial

**How will you get here?**

Education

Bachelor's degree in chemical engineering (or other engineering field), chemistry, pharmacy, or other related science or technical field is required.

**Experience**

- Minimum of one (1) to three (3) years of experience in a manufacturing environment. Experience in product or process development, including scale-up and technology transfer processes for both immediate and controlled release dosage forms preferred.

- Project Management experience with a minimum (1) year of experience.

**Knowledge, Skills, Abilities**

- Understanding of Good Manufacturing Practices (GMP) and regulatory compliance.

- Lead projects of moderate to high complexity in scope and compliance-related challenges to implementing processes to meet changing regulations.

- Proficiency using Microsoft (MS) Office applications.

- Good critical and logical thinking skills. Effective written, interpersonal, and presentation skills, including leading technical discussions with internal and external clients.

- Self-starter, mature, independent, and detailed oriented.

- Ability to work in a fast-paced, results oriented, and structured environment.

- Experience leading projects related to process development including scale-up production activities.

- Effective time management, multi-tasking and prioritization skills to effectively run multiple projects.

- Lead by example.

- Courages and assumes challenges in a risk based approaches.

- Transparent and knowledgeable in presenting project updates daily.

- Diligent in team meetings and discussions.

- Collaborate across multiple departments to reach goals and objectives.

- Inclusive with communication styles and ideas.

- Conscientious to fellow peers with work load requirements.

- Coordinate and lead weekly meetings with customers.

- Fast and focused execution of tasks will be required at time.

- Build helpful ideas to increase production efficiencies.

- Technical skill information transferred to supporting departments.

- Participate and support audit participation and interaction for regulatory agencies.

- Develop and transform learning to peers with technical and mechanical result oriented aptitudes.

- Written communication skills expected and presentation will be expected.

**Physical Requirements:**

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office and manufacturing locations; ability to stand, walk, stoop, kneel, crouch periodically, manipulation (lift, carry, move) of light to medium weights of 10-35 pounds; arm, hand and finger dexterity, including ability to grasp and type for periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

Manufacturing Process Engineer

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

**Discover Impactful Work**

As a member of the Bioprocessing Collaboration Center (BCC), you will develop and drive implementation of innovative upstream bioprocessing solutions! You will act as technical lead on multiple projects. Investigate, create, and develop new scientific methodologies in a cross-company team environment. This role focuses on the evaluation and contribution to the evidence generation of Single Use Technology (SUT) and supporting systems including automation and process analytical technologies. Additionally, you will test novel bioreactors, and control strategies to enhance process intensification and continuous processing strategies as well as drive early adoption of new technologies at both the Pharma Services Group internally as well as at leading biotechnology companies externally.

**Location **: On-site in St. Louis, MO. Relocation assistance is NOT provided.

- Must be legally authorized to work in the United States without sponsorship.

- Must be able to pass a comprehensive background check, which includes a drug screening.

**A Day in the Life**

As a team, we collaborate on experiments showcasing the capabilities and benefits of Thermo Fisher’s technologies! Serve as in-house technical experts in applied biotechnology and process development by working with Process Development and Manufacturing groups to solve process challenges.

As an individual you will conduct sophisticated analyses to support testing and development of SUT systems. Record results in electronic notebook accurately, clearly, and regularly, and reviews documentation by others. Summarize results by preparing internal and externally facing materials such as presentations, protocols, reports, and white papers. Communicate results to people with both technical and non-technical backgrounds.

We also effectively network with colleagues from Bio Design Centers (BDC) and R&D sites globally to build effective shared technical resources and remain current in the field by reviewing relevant scientific literature and attendance at appropriate scientific seminars and conferences. May travel up to 25% as the need arises.

**Education/ Experience**

- B.S. in Chemical Engineering, Biomedical Engineering, Biochemistry, Biology or related field with 5+ yrs, Masters with 3+ yrs, Ph.D. with 1+ yrs.

- Equivalent combinations of education, training, and work experience may be considered.

- Experience with performing standard upstream unit operations (Fed-batch and perfusion cell culture, depth filtration) at bench and pilot scale including AMBR systems.

- Experience with various upstream unit operation control software (DeltaV experience preferred)

- PAT experience preferred

- Automation experience including DeltaV preferred

**Knowledge, Skills, Abilities**

- Advanced and deep knowledge of multifaceted aspects or a specialized aspect of Single Use Technologies and solid understanding of principles of cell culture, including perfusion.

- Excellent problem solving and critical thinking skills. Excellent writing, communication and presentation skills. Strong MS Excel experience. Excellent organization and planning skills.

- Strong attention to detail and ability to adhere to standards procedures.

- Ability to design complex studies and to analyze and summarize scientific data. Ability to author reports, procedures, and other documents. Experience with DOE is preferred.

- Ability to lead and mentor less experienced staff.

- Ability to function in a constantly evolving cross company matrixed environment.

**Physical Requirements:**

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Lift objects up to 50 lbs. occasionally. Stand up to 25% daily. Walk within lab and between buildings daily. Repetitive hand motions.

**What Sets This Opportunity Apart**

- Join a globally renowned company at the forefront of scientific innovation.

- Collaborate with a team of ambitious professionals who are passionate about making a difference.

- Contribute to the success of a company that is dedicated to improving human health and well-being.

- Work in a dynamic and fast-paced environment where your skills and contributions will be valued.

- Access opportunities for professional growth and development within the organization.

At Thermo Fisher Scientific Inc., we are committed to fostering an inclusive and diverse workplace. We are an equal opportunity employer and value the strengths and perspectives that each individual brings to our team. We strive to provide reasonable accommodations and adjustments to applicants and employees with disabilities to ensure equal access to employment opportunities. If you require any accommodations or adjustments during the application process or throughout your employment, please let us know.

Join our exceptional team and take the next step in your career as an executive assistant at Thermo Fisher Scientific Inc. Apply now and seize this remarkable opportunity to contribute to our mission of enabling our customers to make the world healthier, cleaner, and safer.

Apply today! http://jobs.thermofisher.com

Cell Culture Engineer III

**Work Schedule**

Standard Office Hours (40/wk)

**Environmental Conditions**

Office

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

**How will you make an impact?**

Join a team of digital content professionals dedicated to improving how scientists discover and engage with our products and solutions. As a Scientific Digital Content Writer, you will apply your scientific background and digital expertise to create clear, accurate, and high-performing content that supports our customers across the buyer journey.

In this role, you will contribute to content strategy and execution by developing and optimizing web content using SEO and AI-assisted methodologies. You will help ensure content is structured, discoverable, and aligned with user intent, while maintaining the highest standards of scientific accuracy and quality.

You will collaborate with cross-functional partners, incorporate subject matter expertise, and use performance insights to continuously improve content effectiveness. This role requires a proactive, detail-oriented individual who is comfortable working in a fast-paced, matrixed environment and is motivated to learn and apply new tools and processes that drive efficiency and scale.

This is a full-time **on-site **position.

**Key Responsibilities**

- Conduct keyword, topic, and intent research to identify opportunities to drive qualified traffic and engagement

- Develop, write, edit, and optimize scientific and marketing content for web and digital channels

- Apply SEO and AEO best practices to improve content discoverability and performance

- Evaluate existing content to identify duplication, gaps, and optimization opportunities; recommend and implement improvements

- Structure content using clear hierarchies, taxonomy, and internal linking to enhance user experience

- Participate in peer reviews and provide constructive feedback to support content quality and consistency

- Partner with SEO specialists, marketers, and digital teams to support aligned content strategies and initiatives

- Analyze content performance using analytics tools and apply insights to improve results

- Support the adoption of new content workflows, tools, and best practices to drive continuous improvement

- Perform additional duties as assigned

**Education**

- Bachelor's degree required. Biology or a related life sciences field preferred.

- Advanced degree (MS or PhD) in science is preferred

**Experience**

- 3+ years of experience in a life sciences field (e.g., research, R&D, marketing, technical support, or related)

- Experience writing scientific, technical, or marketing content for digital platforms preferred

- Experience working in a matrixed or global organization preferred

**Knowledge, Skills, And Abilities**

- Demonstrated understanding of SEO and emerging AEO principles, with the ability to apply best practices

- Experience using analytics and SEO tools (e.g., Google Search Console, Google Analytics, Adobe Analytics, SEMrush or similar)

- Knowledge of content strategy fundamentals, including information architecture, taxonomy, and user experience

- Comfort using AI-enabled tools to enhance content creation, optimization, and workflow efficiency (no development required)

- Ability to evaluate and refine AI-assisted outputs to ensure scientific accuracy and content quality

- Strong writing, editing, and proofreading skills, with attention to detail

- Effective communication and collaboration skills across cross-functional teams

- Strong organizational skills with the ability to manage multiple priorities and deadlines

**Compensation And Benefits**

The salary range estimated for this position based in California is $75,000.00–$110,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

- A choice of national medical and dental plans, and a national vision plan, including health incentive programs

- Employee assistance and family support programs, including commuter benefits and tuition reimbursement

- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Scientific Digital Content Writer (SEO & AI-Optimized Content)

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

At Thermo Fisher’s PPD clinical research business, we’re using digital innovation, data science, and AI to reimagine how life-changing therapies reach patients. Our teams combine deep scientific expertise with advanced analytics, automation, and digital platforms to make research smarter, faster, and more connected.

We know that innovation happens when diverse minds meet. Our Digital Science, Data, and AI professionals collaborate closely with scientists, clinicians, and operational experts to solve real-world challenges in clinical research. Alongside our partnership with Open AI, you can be part of the collaboration that will help to improve the speed and success of drug development, enabling customers to get medicines to patients faster and more cost effectively.

You’ll join a culture that values experimentation, learning, and collaboration — where your ideas can help shape how we deliver life-saving solutions and improve global health outcomes. Whether you’re a data engineer, product manager, software developer, or AI scientist, you’ll find opportunities here to apply your skills to work that truly matters — improving global health outcomes.

**POSITION SUMMARY:**

The **Senior Director, Software Engineering **, leads a global engineering group responsible for delivering secure, reliable, and differentiated digital products. This leader defines engineering strategy, establishes strong operating mechanisms, and builds a high-performance culture grounded in customer outcomes, quality, and predictable delivery. The role partners closely with Digital Product Management, UX, Data Science, Security/Compliance, and business leaders to translate strategy into scalable platforms and exceptional end-user experiences while accelerating execution through modern engineering practices and AI-enabled productivity.

**Key Responsibilities:**

**Engineering Leadership **:

- Define and implement strategic technical direction and engineering best practices.

- Foster a culture of quality, accountability, innovation, and continuous improvement within the engineering teams.

- Oversee the architecture and technical decisions, ensuring solutions are scalable, secure, and align with the organization’s long-term vision.

- Stay abreast of AI and machine learning technologies to optimize engineering workflows, enhance developer productivity and streamline development processes.

**Global Talent Development and Management **:

- Recruit, mentor, and retain high-performing engineering talent.

- Drive career development, set clear performance objectives, and establish a supportive environment for professional growth.

- Manage growth and expansion of engineering capabilities in strategic global locations.

- Provide coaching, leadership, and technical guidance to engineering teams and managers.

**Engineering Excellence:**

- Lead the adoption and execution of modern software development methodologies (e.g., Agile, CI/CD, DevOps, Cloud-native practices).

- Establish robust QA practices, including automation and testing strategies, to ensure delivery of reliable and high-quality software products.

- Ensure adherence to industry standards, compliance regulations, security best practices, and performance benchmarks.

**Collaboration and Stakeholder Engagement:**

- Collaborate closely with stakeholders to ensure alignment on product goals, timelines, and deliverables.

- Clearly communicate engineering strategies, plans, and progress to executives, stakeholders, and cross-functional teams.

- Act as a trusted advisor on technical matters to senior leadership and peers across the organization.

**Operational Excellence:**

- Manage budgets, resource planning, and vendor relationships related to engineering activities.

- Implement metrics-driven management, defining clear KPIs to measure team performance, product delivery success, and operational effectiveness.

- Proactively manage risks and challenges, driving prompt resolution to maintain timelines and quality.

______________________________________________________________________________

**Required Qualifications:**

- Bachelor’s degree required; advanced degree in healthcare, life sciences, computer science, business, or related field preferred.

- Progressive engineering leadership experience that provides the knowledge, skills, and abilities to perform the job (comparable to 12+ years’ experience)

- 5+ years in leadership roles managing software engineering teams.

- In some cases, an equivalency, consisting of appropriate education, training, and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.

**Preferred Experience:**

- Experience leading engineering teams in a product-driven, customer-centric environment.

- Background in healthcare, clinical research, life sciences, or related regulated industries (desirable but not required).

- Proven success in establishing new functions or scaling early-stage engineering teams within large, complex organizations.

**Knowledge, Skills, and Abilities:**

- Proven experience driving large-scale digital transformations and building robust, scalable platforms.

- Demonstrated expertise in modern software development practices, cloud technologies, microservices architecture, DevOps practices, and security frameworks.

- Strong track record in talent development, mentoring, and building high-performing teams.

- Excellent communication and collaboration skills, able to clearly articulate complex technical concepts to both technical and non-technical stakeholders.

At Thermo Fisher Scientific, we are committed to fostering a healthy and harmonious workplace for our employees. We understand the importance of creating an environment that allows individuals to excel. Please see below for the required qualifications for this position, which also includes the possibility of equivalent experience:

- Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.

- Able to work upright and stationary for typical working hours.

- Ability to use and learn standard office equipment and technology with proficiency.

- Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

- May require as-needed travel (0-25%).

Location: Remote US (East Coast preferred). Relocation assistance is NOT provided.

- Must be legally authorized to work in the United States without sponsorship.

- Must be able to pass a comprehensive background check, which includes a drug screening.

The annual salary range estimated for this position in North Carolina is $160,000- $240,000 USD. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.

Senior Director, Software Engineering

**Work Schedule**

**Other**

**Environmental Conditions**

Office

Join us as a Scientist!

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.

**Essential Qualifications:**

-  Bachelor’s degree in Packaging Engineering, Packaging Science, Chemistry, Life Science, with 2-4 years’ experience in parenteral package development, primarily in pharmaceutical industry

-  Analytical and/or lab based experience in the pharmaceutical industry

Preferred Qualifications:

-  Knowledge of parenteral packaging materials, components, vendors, analytical equipment, and technologies.

-  Experience in sterile drug primary packaging development for large and small molecules including vial/stopper, pre-filled syringes, and cartridges presentations.

-  Knowledge of domestic and international packaging requirements and regulations (i.e., current applicable FDA/MAA guidelines, USP/Ph Eur, etc).

-  Knowledge of statistical analysis and Design of Experiments as they apply to packaging operations.

-  Ability to quickly establish relationships with internal and external stakeholders.

-  Strong time management / organizational skills.

-  Evidence of team working skills and flexibility.

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

**Work Summary:**

To provide packaging development analytical support in the UP, PA site.

The task list outlined below provides a comprehensive summary of the crucial work that needs to be carried out in the Steriles Packaging Development lab/team. This work is primarily aimed at offering support for a multitude of projects related to Steriles ViiV projects in development at GSK.

**Tasks:**

-  Perform timely execution of lab based analysis, including experiment write up to support sterile primary package selection, integrity, stability, and lifecycle for the coordination and testing of samples

-  Examples of analytical technique include extrusion force testing, stopper movement assessment, CCI capabilities including HeLD, Vacuum Decay, and headspace analysis

-  Be a practical expert in a packaging/analytical technique relevant to a primary pack presentation, capable of training others in the technique and application

-  Collaborate with the Lab Manager to maintain the License To Operate (LTO) status in the Lab – including equipment maintenance, documentation and coordination with vendors, management monitoring, and safety requirements

-  Maintain packaging lab component and lab inventory, including ordering, receiving, and organization of lab space to enable dynamic, flexible laboratory workspace

-  Prepare and communicate data summaries to relevant project team members

**Stretch Tasks:**

-  Writing work instructions, study protocol contribution

-  Authoring/revising component specifications

-  Supporting document and knowledge management

**Working Conditions and Environment:**

-  Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.

-  Occasional drives to site locations, occasional domestic travel.

-  Exposure to biological fluids with potential exposure to infectious organisms.

-  Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.

-  Personal protective equipment required such as protective eyewear, garments and gloves.

-  Exposure to fluctuating and/or extreme temperatures on rare occasions.

**Physical Requirements:**

-  Ability to work in an upright and /or stationary position for 6-8 hours per day.

-  Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.

-  Occasional mobility needed.

-  Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

-  Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

-  Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

-  Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

-  Frequently interacts with others to obtain or relate information to diverse groups.

-  Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.

-  Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

-  Regular and consistent attendance.

**Why Join Us?**

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Scientist: Steriles Packaging Development

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