Scientist - Bioanalytical LCMS Research and Development

About the role

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.

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.

Responsibilities

Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Possesses an understanding of laboratory procedures and with increased independence over time can conduct complex analysis. Performs a variety of routine 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.

Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. 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. 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.

Completes QA facing tasks with minimal supervisor/QA input. Authors low complexity quality records and participates in the OOS/OOT/Atypical investigation process.

Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years)
• OR a Master’s degree
• 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

Skills

• Knowledge of routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory guidelines
• Knowledge of applicable regulatory authority, compendia and ICH guidelines
• Demonstrates excellent manual dexterity skills, allowing for precise and accurate work
• Exhibits strong written and oral communication skills, facilitating effective 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
• Capable of cross-training on sample preparation techniques with another laboratory group, enhancing versatility and collaboration
• Thrives in a collaborative work environment, actively contributing to a cohesive and productive team
• Demonstrates behaviours which align to the 4i Values of Thermo Fisher

Working Conditions and Environment

This is a fully onsite role based at our 8700 Quioccasin Road location in Richmond, VA. 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.

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 and/or standing for typical working hours. Able to lift and move objects up to 25 pounds.

Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.

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

Benefits

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

Pay

The hourly pay range estimated for this position based in Virginia is $28.00–$29.00. 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.