About the roleAs supervisor, you will manage a team of approximately 30 members, including process operators, cleanroom leads, badge record reviewers and experts.Responsibilities include overseeing daily operations, conducting one-on-one and evaluation meetings, participating in recruitment interviews, and collaborating with schedulers for planning. The position operates on a 4/4 shift system with 10-hour shifts.Key responsibilities
Manage operational teams and supervise various units within the CAR-T production process
Ensure strict compliance with cGMP standards and manage quality aspects
Collaborate with other departments to resolve production issues effectively
Oversee and review critical documentation such as procedures and work instructions
Supervise the release and review of batch records for quality control
About you
Preferably a PhD or Masters degree in science, bio-engineering, pharmacy or other related fields
Min 3 years of experience in a GMP or ATMP environment (preferably within the pharmaceutical or biotech industry)
Knowledge regarding cGMP regulations and clean room operations is an advantage
Familiarity with MES (Manufacturing Execution Systems) & ERB (Electronic Batch Record) is a plus
