QC Analyst

Belgium | QC Analyst | QC Testing | GMP | Environmental Monitoring | Documentation | 1048582

Your new company

Our client, in Belgium, is a global biotechnology company dedicated to treating and curing life-threatening diseases. They develop cell therapies across a diverse range of technology platforms, including autologous and allogenic chimeric antigen receptor T – cell and NK cell – based immunotherapy. They are committed to improving the lives of patients worldwide at multiple sites and their goal is to reimagine healthcare and to deliver transformative treatments in the fields of oncology and cell therapy.


Your new role

We are searching for a passionate and motivated QC Analyst to join our client in Belgium. As a QC Analyst you will be responsible for:
  • Advanced QC Testing: You will perform QC testing for CAR-T products in IPC laboratories and ensure compliance with all procedures, standards and GMP regulations.
  • Environmental monitoring: You verify clean room classification by taking samples of (non-) viable particles and microorganisms.
  • Collaboration: You will work closely with the Quality and Operations departments to bring analytical testing from the test bench to production.
  • Documentation and data management: You will review and approve QC data, maintain process integrity through accurate documentation, and manage test results in our eLIMS software.
  • Process Optimisation: You will create and review QC documents, SOPs and work instructions and also contribute to process optimisation.


What you'll need to succeed

The successful candidate will have at least a bachelor's degree in lab technologies or other related field, or equivalent experience.
Practical experience in an aseptic production facility within QC or QA is a plus but certainly not a must. The client will offer you the necessary training to get you started in your new role. You should have knowledge of cGMP regulations and FDA/EU guidelines and experience in Microsoft Office applications such as Outlook, Excel, Word and PowerPoint. You are fluent in Dutch or English, with strong oral and written communication skills. Practical experience with aseptic processing in ISO 5 clean rooms, familiarity with CAR-T QC testing methods and Good Tissue Practices is a plus. You must be in the Ghent region or have affiliation with the area. Perhaps you have family there or connections from studies.


What you'll get in return

Our client in Belgium is offering contracts directly so you will sign your contract with them. After successful interview rounds and offer acceptance, you will get a meaningful job that contributes directly to the well-being of patients with an excellent work-life balance. You’ll be part of a supportive and innovative working environment that encourages learning and personal development. Alongside that, you will get the chance to work in a multinational setting with an open – ended contract and an attractive salary package (3264 bruto per month excl. shift allowance). You will be working in a shift schedule, working 4 days on with 4 days off and night shifts are expected of you in this role. Other secondary benefits include additional statutory vacations, meal vouchers, group and hospitalisation insurance, an end-of-year bonus and performance bonus.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.


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Overzicht

Contractvorm
Permanent
Branche
Industrieel & Productie
Locatie
Ghent, Belgium
Vakgebied
Life Sciences
Salaris
€3264 bruto per month ex. shift allowance
Referentie:
1048582

Spreek met een consultant

Spreek met Eibhlin Hanlon, de recruiting expert die deze vacature in behandeling heeft, werkzaam in kantoor Amsterdam
Hays Amsterdam, Rijnsburgstraat 9-11

Telefoonnummer: 0615868143