Help shape the future of CAR-T therapies by bringing your QA expertise to innovative MES automation projects in Belgium. Join a dynamic international team and make an impact on life-saving treatments.
What is offered
Ready to grow your career and make real impact? Join MindCapture!
We offer competitive salaries, a full benefits package (meal vouchers, eco vouchers, DKV health insurance, group insurance, net expense allowance, and a company car) — plus the opportunity to shape your future through personalized training and development.
At MindCapture, you choose what you love, build on your strengths, and make a difference where it matters most.
You will work as a MindCapture consultant for an international market leader in the healthcare industry.
Job Description:
* Ensure QA oversight in MES (Manufacturing Execution System) projects for CAR-T manufacturing sites in Ghent and Beerse
* Transform paper-based documentation into electronic master batch records together with production, engineering and IT teams
* Review and support validation deliverables (protocols, traceability matrices, test scripts)
* Ensure compliance with GMP and regulatory standards through risk assessments, change controls and audits
* Collaborate with international partners and contribute to lean automation and continuous improvement initiatives
Requirements:
* Degree in Bio-Engineering, Industrial Pharmacy or technical field (Engineering, Computer Science, etc.)
* At least 2 years of experience in the pharmaceutical industry
* Strong knowledge of GMP and QA in production environments
* Experience with master batch records and/or MES systems is a strong asset
* Analytical, solution-oriented and collaborative team player
* Fluent in English AND Dutch or French (spoken and written)
Are you ready to make a real difference in healthcare?
Join our dynamic team and help drive innovation in biotech.
Apply now and let’s make an impact together!
Want to learn more? Discover all opportunities at www.mindcapture.com.