Bachelor’s Degree in cell biology, biotechnology, biochemistry, microbiology, life sciences, or equivalent with a minimum of 4 years of relevant experience in biologic or cell therapy.
Knowledge of regulatory requirements, including current Good Manufacturing Practices (cGMP), Good Practices (GxP), 21 CFR Part 11, Good Documentation Practices (GDP), and Annex 1.
· Excellent observational, documentation, and communication skills.
· Ability to work independently and collaboratively in a fast-paced environment.
· Experience with training or coaching operators is a plus.
Experience with ergonomics relating to aseptic techniques and aseptic behaviors.
Experience with electronic quality management systems.
Experience with cleaning and sanitization practices.
· Certification in aseptic processing or quality assurance.
· Experience with sterile injectable products.
· Experience with electronic quality systems.
· Knowledge of cGMPs. Cell therapy and aseptic processing experience is required.
· Ability to collaborate and influence cross-functional teams.
· Experience with leading change management is preferred.
WORKING CONDITIONS (US Only):
· Must be able to work in a cleanroom environment that requires gowning within ISO 5/7 (Grade A/B).
· Must be able to stand for extended periods of time.
· Work in areas that may have strong magnets.
· Work in areas where handling human blood products (Biosafety Level 2) may be required.
· May work in areas with exposure to vapor phase liquid nitrogen.
· Must be able to gown in and be present in the Grade A/B environment for extended periods of time.