What are the responsibilities and job description for the Clinical Trial Supply Expert position at Thermo Fisher Scientific Careers?
Job Description
The Analytical Scientist Position involves working in a regulated cGMP lab environment with responsibilities that include:
- Analytical characterization and assessment of clinical trial supplies.
- Understanding corporate standards regarding code of conduct, safety, and GxP compliance.
- Responsible for compliance with all applicable Client policies and procedures.
- Documenting experimental data appropriately in laboratory documentation systems.
- Maintaining laboratory equipment and optimizing laboratory operations for safe and efficient use of time and resources.
Key Skills and Qualifications
- Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology, or similar.
- Previous experience providing knowledge, skills, and abilities to perform the job, comparable to 2 years, or Master's degree.
- Experience in a regulated cGMP Lab.
- Experienced in laboratory systems (LIMS, CDS, ELN) required.
- A full understanding of laboratory requirements, PPD & client SOPs, ICH guidelines, USP requirements, and FDA guidance.
