Operations Advanced Support Supervisor - Life Sciences - M/F/X
Permanent Contract
31 Oct 2025
Flandre orientale
Verified by Turrior
Content + Source + Freshness • 18 Dec 2025 • 95% confidence
78 / 100
Offer value
Moderate value level mainly due to specialized skills required in a niche industry and potential for career advancement in a high-demand field.
- Involves leadership of large production teams
- Engagement in CAR-T process, a cutting-edge treatment method
- Requires 5+ years of management experience
Pros
- Opportunities to lead a sizable team in a specialized industry
- Involvement with state-of-the-art CAR-T manufacturing processes
- Potential for skill development in compliance and EHS
Cons
- The shift work may not appeal to everyone
- High accountability could lead to stress
- Limited sitting at desk time, mainly active on production floor
Who it's for
Mid-level to Senior • On-site with shift work
Good fit
- Experienced professionals in life sciences management
- Leaders from regulated industries familiar with compliance
- Individuals excited about innovative health technologies
Not recommended for
- New graduates or those without leadership experience
- Candidates looking for a strictly 9-to-5 work schedule
- Individuals uncomfortable in dynamic and fluctuating environments
Motivation fit
Desire to improve team performance in high-stakes environmentsInterest in process optimization and complianceWillingness to thrive under shifting operational demands
Key skills
Expertise in cGMP and ATMP proceduresStrong leadership and communication skillsFamiliarity with production documentation and standard operating procedures
Score: 78/100 AI verified analysis
About the job
About the role
An Operations Advanced Support Supervisor will oversee the support operations team responsible for production support activities, including Grade B cleaning, Material Transfer, Replenishment and Sterilization.
The role involves managing aspects of the CAR-T process operations, ensuring safe and compliant manufacturing operations in line with cGMP requirements. The position operates on a 4/4 shift system with 10-hour shifts.
Key responsibilities
- Act as a SME for quality aspects related to production activities
- Manage and review documentation in Production zones, including batch records and SOPs
- Lead and coordinate production support activities, optimizing schedules for compliance
- Support Tech Transfer plans for new production introductions and process optimizations
- Implement and lead Tier 1 and Tier 2 meetings to ensure clear communication
- Ensure safe and compliant operations according to EHS and cGMP
About you
- Bachelor or Master in science, bio-engineering, pharmacy or related field
- Min of 1 year in a cGMP or ATMP environment
- Min of 5 years of direct people management, overseeing teams of 10+ individuals
- Proficiency with Microsoft Office tools, MES/EBR knowledge is a plus
- Fluency in English and Dutch
- Ability to accommodate shift work, including evenings and weekends as required
