QA Specialist – QA Operations, Drug Substance

EFOR; Geel; Sur place; EUR 47 000 - 60 000; Plein temps

Résumé du poste

EFOR Group, a trusted Life Sciences partner, seeks a QA Specialist on client site in Geel, Belgium, to provide quality oversight in QA Operations for a multiproduct Drug Substance facility.

You will review batch records, approve SOPs, manage quality documents, and oversee alarms, leveraging cGMP knowledge and strong attention to detail.

Qualifications

• Master's degree in a scientific field or equivalent through relevant experience.
• Thorough knowledge of and experience interpreting cGMP guidelines in a regulated environment, with particular attention to data integrity.
• Knowledge of clinical manufacturing and its associated regulations is a plus.
• Experience with Quality processes and Quality Assurance.
• Experience with batch record review.
• Excellent accuracy and attention to detail.
• Independent working style with initiative and ownership.
• Enthusiastic team player with strong communication skills.
• Strong writing skills and clear written expression.

Responsabilités

• Perform quality reviews of batch records and logbooks, both electronic and paper-based.
• Issue and archive paper-based batch records, logbooks, and other operational documents requiring quality oversight.
• Review and approve operational documents (SOPs, forms, etc.) requiring quality oversight.
• Take ownership of quality documents (SOPs, forms, etc.).
• Provide quality oversight in the management of alarms.

Connaissances

Quality assurance

cGMP knowledge

Data integrity

Communication skills

Attention to detail

Independent working

Team player

Writing skills

Formation

Master's degree in a scientific field

Description du poste

? Now Hiring: QA Specialist – QA Operations, Drug Substance (Geel, Belgium | Contract)

Are you a meticulous QA professional ready to provide quality oversight within a multiproduct Drug Substance manufacturing facility? EFOR Group, a trusted Life Sciences consulting partner, is seeking a skilled QA Specialist to join our team on a client site in Geel, Belgium, within the QA Operations department of a globally leading biopharmaceutical company.

? Contract duration: 01/10/2026 – 31/12/2026

In this role, you'll play a key part in ensuring the quality and compliance of operational processes and documentation across a multiproduct Drug Substance (DS) production facility.

What you'll do:

• Perform quality reviews of batch records and logbooks, both electronic and paper-based
• Issue and archive paper-based batch records, logbooks, and other operational documents requiring quality oversight
• Review and approve operational documents (SOPs, forms, etc.) requiring quality oversight
• Take ownership of quality documents (SOPs, forms, etc.)
• Provide quality oversight in the management of alarms

Your background:

• Master's degree in a scientific field, or equivalent through relevant experience
• Thorough knowledge of and experience interpreting cGMP guidelines in a regulated environment, with particular attention to data integrity
• Knowledge of clinical manufacturing and its associated regulations is a plus
• Experience with Quality processes and Quality Assurance
• Experience with batch record review
• Excellent accuracy and attention to detail
• Independent working style, with initiative and a strong sense of ownership
• Enthusiastic team player with strong communication skills
• Strong writing skills and clear written expression

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 biopharmaceutical site?