QA Document Control

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.