Assistant Scientist - Vaccines (Four 10 - Hour Shifts)

Thermo Fisher Scientific•Richmond, VA

15h•Onsite

About The Position

Position : Assistant Scientist ( Four 10-hour shifts - Saturday + 3 weekdays of your choice) Location : Richmond, VA Department : Vaccines This is a fully onsite role based at our BIOA Laboratory 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. 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. Location/Division Specific Information Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic authorities. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. A day in the Life: 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. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Communicates project status to project leader. Maintains a laboratory notebook and completes all laboratory documentation in clear and accurate language and according to SOP and GLPs. Performs daily work assignments accurately, and in a timely and safe manner. Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.

Requirements

Bachelor's degree in health/life sciences (Biology, Chemistry, Biochemistry, etc) o r equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 years).
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.
Experience with analytical assays such as immunoassays, ELISA, or similar testing methods
Training or experience in microbiology, cell culture, or molecular biology techniques
Knowledge of aseptic and sterile techniques and ability to work in regulated laboratory environments (e.g., BSL I/II, biosafety cabinets, fume or flow hoods)
Adherence to laboratory safety standards, including proper use of PPE and compliance with safety procedures
Knowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines
Knowledge of applicable regulatory authority, compendia and ICH guidelines
Demonstrated manual dexterity and ability to operate laboratory equipment (e.g., pipetting, routine lab instrumentation)
Good written and oral communication skills
Time management and project management skills
Proven problem solving and troubleshooting abilities
Ability to cross-train on sample preparation techniques with another laboratory group
Ability to work in a collaborative work environment with a team

Responsibilities

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.
Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines.
Communicates project status to project leader.
Maintains a laboratory notebook and completes all laboratory documentation in clear and accurate language and according to SOP and GLPs.
Performs daily work assignments accurately, and in a timely and safe manner.
Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.