Operations Advanced Supervisor - Life Sciences - M/F/X
Permanent Contract
14 Nov 2025
Flanders, Belgium
Verified by Turrior
Content + Source + Freshness • 18 Dec 2025 • 95% confidence
80 / 100
Offer value
High value due to leadership opportunities, team management responsibilities, and critical involvement in production processes.
- Lead a large team in CAR-T production.
- Strong focus on compliance and quality assurance.
- Provide significant impact on operation efficiency.
Pros
- Leadership role with the opportunity to develop team dynamics.
- Involved in cutting-edge CAR-T production yields high relevance.
- Intensive training and professional development available.
Cons
- High-pressure environment due to regulatory requirements.
- Obligatory shift work may affect work-life balance.
- Experience requirement may limit suitable candidate pool.
Who it's for
Senior / Lead • On-site, shift work
Good fit
- Experienced leaders in life sciences
- Individuals passionate about team dynamics and efficiency
- Candidates seeking robust growth within biotech
Not recommended for
- Newcomers without supervisory experience
- Candidates seeking standard office hours
- Those opposing regulatory-intensive environments
Motivation fit
Desire to oversee operational excellence in production.Interest in managing large teams and improving processes.Eagerness to work in high-stakes environments.
Key skills
Team managementcGMP complianceOperational troubleshootingDocumentation review
Score: 80/100 AI verified analysis
About the job
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)
