Start People is recruiting for a biotechnology company in Ghent a QA Document Control Specialist.
In this role, you will support and manage document control processes in a sterile GMP environment, linked to cell therapy manufacturing for both clinical and commercial purposes.
Key responsibilities include:
* Managing document control systems and reviewing procedures.
* Supporting users of the electronic document management system.
* Issuing and reconciling GMP documentation.
* Archiving and managing the document lifecycle.
* Driving continuous improvement and compliance with regulatory standards.
Profile sought:
* Secondary or higher education, or equivalent through experience.
* Previous GMP experience is an advantage, but not mandatory.
* Strong communication skills in Dutch and technical English.
* Detail-oriented, organized, and able to handle shifting priorities.
Schedule: Day shift (8am–6pm), 4 days per week (10h/day). There is a possibility of moving to a 2-shift system (early and late) mid/end 2026.
We offer:
* Initial interim contract with permanent contract after 6 months.
* Attractive salary package with extra benefits: meal vouchers, group and hospitalization insurance, extra vacation days, performance bonuses.
* A supportive and innovative multicultural work environment that fosters professional growth.