Quality Officer – Biotech, Remote‑Friendly Role

Agomab; Antwerpen; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

Agomab is seeking a Quality Officer to join the expanding Quality team in Antwerp. The role reports to the Head of Quality and focuses on maintaining and improving the quality management system, document control, and providing practical quality support across the organisation.

The ideal candidate has a bachelor’s degree in life sciences and at least three years of quality experience in biotech/pharma, with hands-on GMP/GCP knowledge and experience with electronic quality management systems.

Qualifications

• Minimum three years of quality experience in biotech/pharma.
• Hands-on knowledge of GMP and/or GCP quality systems.
• Experience with electronic quality management systems.

Responsibilities

• Act as a key Quality contact across Agomab, providing guidance to colleagues.
• Support development and maintenance of the quality management system, including procedures and training.
• Coordinate document control activities and review operational documents from a quality perspective.
• Facilitate risk management, change control, non-conformance investigations and CAPAs.
• Plan internal audits and self-inspections, and support external audits and regulatory inspections.
• Contribute to management review meetings preparation and follow-up.
• Support validation and lifecycle management of electronic systems, including periodic reviews.
• Champion continuous improvement and a culture of compliance.

Skills

Quality management

GMP/GCP knowledge

Electronic quality systems

Education

Bachelor’s degree or higher in life sciences or related discipline

Job description

Agomab is seeking a Quality Officer to join the expanding Quality team in Antwerp. The role reports to the Head of Quality and focuses on maintaining and improving the quality management system, document control, and providing practical quality support across the organisation.

The ideal candidate has a bachelor’s degree in life sciences and at least three years of quality experience in biotech/pharma, with hands-on GMP/GCP knowledge and experience with electronic quality management systems.