Scientist - Labs - QC Stability

at  Thermo Fisher Scientific

JOB DESCRIPTION

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.
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

EDUCATION AND EXPERIENCE:

• Bachelor’s degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar
• Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’)
• OR Masters 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.

KNOWLEDGE, SKILLS AND ABILITIES:

• Past experience with Quality Control, preferably with focus on stability
• Good understanding of cGMP, GDP and GLP regulations and guidelines
• Knowledge of clinical and commercial QC stability regulations (FDA, EMA, ICH)
• General experience in data analysis and statistical evaluation/data trending

Managing routine operations of the cell banks, critical intermediates, Drug Substance and Drug Product. Clinical GMP stability programs of cell and genetic therapies while ensuring compliance with SOPs. In addition, this role will be responsible for supporting various GMP stability testing programs and Quality Systems, handling stability Quality Events, performing stability testing, delivering stability documents.

• Draft and revises stability protocols and reports, from initiation to finalization
• Creates and maintains stability schedules for GMP clinical stability studies, ensuring stability samples get pulled within appropriate timeline
• Coordinate with external testing labs to retrieve stability testing data and timepoint reports
• Initiate, document and address stability quality events, including change controls, deviations, and analytical investigations.
• Update stability related GMP documents (specifications, JoS, memos, etc.)
• Performs initiation and management of stability studies in LIMS and performs data entry and review.
• Support continuous improvement activities for stability program.