• Support Qualified Persons in all GMP administration tasks to meet departmental objectives;
• Maintain batch manufacturing record files according to storage procedures;
• Store, manage and track company documentation in MYCIM or Vault;
• Ensure compliance to GMP;
• Ensure that all necessary steps have been completed under accepted pharmaceutical quality systems to assure compliance of the batch records with GMP;
• Working with other departments and communicate internally and externally effectively.
• Continuous Improvement - Support review of release processes for simplification.
• Executes on decisions made according to written procedures and standard practices.
• Communicate appropriately any identified issues.
• MLO or HBO (BSc) degree in Biology, Biochemistry, Life Sciences or related sciences;
• 2 years experience with GMP is preferred;
• You enjoy working in a team and communicate well;
• You are flexible and proactive;
• You are accurate, and have great attention to detail;
• You are fluent in English and Dutch (Spoken/written)
• A market competitive salary;
• Benefits that include yearly bonus, cycling plan, discount on your fitness subscription, 31 vacation days, etc.;
• Specialist training and a range of opportunities for personal and professional development;
• A company well-being program targeting both mental and physical well-being;
• A fantastic team with monthly team lunches, fun teambuilding activities (laser tag, escape rooms, sports, etc.) and above all; a great collaborative work environment.
Interested and more information?
For questions about the position, please follow the "I'm interested" link below to contact the appropriate manager.
Acquisition in response to this vacancy is not appreciated.
