About the role

As 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
• You are fluent in English (spoken & written)