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.