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QC Supervisor
Requirements:
QC Supervisor
Location | Gent |
Job type: | Permanent |
Contact name: | Bob Beevers |
Contact email: | [email protected] |
Contact phone: | |
Job ref: | 28509 |
Published: | 3 days ago |
Expiry date: | 07 Sep 2023 11:59 |
QC Supervisor
Gent/Ghent, Belgium
Shifts – 4 on 4 off
Dutch & Technical English Required
A leading commercial stage biotech business based in Gent are keen to bring onboard a QC Supervisor to head up their on-site Quality Control Operations. This organisation is a leader within cell based therapy and is keen to expand upon their commercial success by expanding their site operations. Part of this growth involves bringing a QC Supervisor into their growing team.
The QC Supervisor will be responsible for ensuring quality control over personalised cell therapy for both clinical and commercial use in a sterile GMP environment. The successful QC Supervisor will manage a team of 8-10 QC Analysts and will be responsible for all troubleshooting.
Responsibilities:
- Managing team of analysts, including setting shift patterns, supporting team member development and leading on all troubleshooting
- Building strong internal relationships with Quality Assurance, IT, HSE, Maintenance, HR & Manufacturing Teams
- Responsible for both in process analyses and environmental monitoring
- Ability to read, interpret and revise documents such as SOPs, work instructions
- Independently makes appropriate and compliant GMP decisions
- Independently resolves problems through the use of quality systems
- Develop improvement ideas and independently implement associated solutions
- Supports the completion of corrective and preventive actions
Requirements:
- Degree educated in Science or related subject, equivalent technical experience would be considered
- Strong work experience, ideally 6+ years operating within an aseptic manufacturing facility
- Experience operating within Quality Control
- Management or Supervisory experience of minimum 1 year required
- Strong knowledge of cGMP, and FDA/EU guidelines relating to manufacturing and QC of cell based products. Knowledge of Good Tissue Practices is beneficial. Experience with ICH and/or CFR.
- The site speaks Dutch and Technical English, both are required for this position.
If this sounds like an ideal next step in your career, please apply online.
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