Are you a quality-minded professional with a sharp eye for GMP documentation? EFOR Group, a trusted Life Sciences consulting partner, is seeking a skilled Quality Officer to join our team on a client site in Geel, Belgium, providing temporary support on batch-related documentation in a GMP environment.
? Contract duration: 14/09/2026 – 31/12/2026
The focus of this assignment is on QA review of batch-related documentation.
What you'll do:
- Perform QA review of batch-related documentation in line with GMP requirements
- Work within the site's QMS systems to ensure documentation accuracy and compliance
- Support MES-related batch review activities
- Collaborate closely with cross-functional teams to keep documentation flow on track
Your background:
- Bachelor's or Master's degree in a scientific field
- Experience working in a GMP environment
- Experience with QMS systems
- Experience with MES; familiarity with Inova is a plus
- Strong communication skills
- A collaborative team player
Why EFOR Group?
EFOR unites over 3,200 experts in 18 countries, delivering unparalleled technical, quality, and engineering excellence across the full Life Sciences product lifecycle. Join a high-performing team committed to healthcare innovation, safety, and reliability.
? Location: Geel, Belgium
? Ready to bring your quality expertise to a leading pharmaceutical site?