Company Description
Eurofins is Testing for Life.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing, and in discovery pharmacology, forensics, advanced material sciences and agro-science Contract Research services. Eurofins is also a market leader in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in Biopharma Contract Development and Manufacturing. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. With 58,000 staff across a network of 900 laboratories in 54 countries, Eurofins' companies offer a portfolio of over 200,000 analytical methods. Eurofins Shares are listed on Euronext Paris Stock Exchange.Eurofins PSS Insourcing Solutions®
is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client' site, utilizing their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!Job Description
• 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.
Qualifications
• 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)
Additional Information
• 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?
Acquisition in response to this vacancy is not appreciated.