Senior Scientist, Chromatography

Thermo Fisher Scientific · Richmond

Apply on the company website

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

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

Job Description

Join us as Senior 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.

As a Senior Scientist, your role will be to conduct advanced diagnostic tests, ensure the highest accuracy and reliability of laboratory data, mentor junior scientists, and drive continuous improvements in laboratory methodologies and quality standards.

What You’ll Do:

Trains on routine operation, maintenance, and theory of complex 
analytical instrumentation, SOPs, and regulatory procedures and 
guidelines.
• Independently performs and gives guidance on a variety of routine to 
complex sample preparation and analysis procedures to 
quantitatively measure pharmaceutical and biopharmaceutical 
compounds in a variety of formulations and/or biological matrices for 
stability and analytical testing.
• Completes all laboratory documentation in clear and accurate 
language and according to SOP and GLPs.
• Independently troubleshoots equipment & instruments. Mentors’
others in troubleshooting when applicable.
• Reviews and compiles results from assignments and makes initial 
determination on acceptability per SOP acceptance criteria. Navigates 

the OOS/OOT/Atypical investigation process. Leads investigations and
Root Cause Analysis and proposes CAPAs.
• Performs work assignments accurately, and in a timely and safe
manner.
• Independently manages QC responsibilities. Communicates project
status to project leader and helps to identify gaps and anticipates
roadblocks in project team workflow.
• Coordinates laboratory activities of other team members in
conjunction with the lab supervisor.
• Assists with the study design & protocol authoring. Leads data
evaluation and study close-out.
• Independently completes QA facing tasks. Authors and leads more
complex quality records (eg. quality records which may require more
in-depth investigation to identify true root causes, quality records
requiring cross-departmental input and/or collation of data etc.)
Education and Experience:

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:

Knowledge of routine operation, maintenance, and theory of analytical instrumentation,
SOPs, and applicable regulatory authority, compendia and ICH guidelines and ability to
interpret and consider SOP and regulatory guidelines during study design activities
• Ability to understand and independently apply GMPs and /or GLPs to everyday work
with regard to documentation and instrument use

communication within the team and with stakeholders.
• Displays exceptional time management and project management skills, ensuring
efficient completion of tasks.
• Proven problem-solving and troubleshooting abilities, enabling the identification and
resolution of issues.

group, enhancing versatility and collaboration.
• Thrives in a collaborative work environment, actively contributing to a cohesive and
productive team.
• To demonstrate behaviors which align to the 4i Values of Thermo Fisher



Working Conditions and Environment:



Physical Requirements:

the fingers, hands, and wrists.

computer with a maximum lift of 15-20 lbs.

understand information and ideas presented through spoken words and sentences.

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.

Compensation and Benefits

The salary range estimated for this position based in Virginia is –.

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:

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

More jobs at Thermo Fisher Scientific · Other jobs in Richmond