Scientist - Data Reviewer - Bioanalytical LCMS Assay Services - M - F Second Shift

Work Schedule Second Shift (Afternoons) Environmental Conditions Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description 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.  This position will work Monday to Friday 2:30 p.m. to 11 p.m. EST. 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. Discover Impactful Work: 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. A Day in the Life: Trains on routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines.  Performs a variety of routine to complex sample preparation and analysis procedures with minimal supervision/guidance 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.  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.  Keys to Success:

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+