Quality Officer

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

Quality Officer

Department: Quality

Employment Type: Permanent - Full Time

Location: Agomab Antwerp

Description

As Agomab advances its clinical-stage pipeline, we are seeking a Quality Officer to join our growing Quality team and report to the Head of Quality. In this hands-on role, you will help maintain and continuously improve our quality management system, take ownership of document control, and provide practical quality support across the organisation.

Key Responsibilities

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

Skills, Knowledge and Expertise

• A bachelor’s degree or higher in life sciences or a related discipline.
• At least three years of relevant Quality experience in a biotechnology or pharmaceutical environment.
• Demonstrated knowledge of GMP and/or GCP quality systems, supported by recent training or certification.
• Hands-on experience with electronic quality management systems and their ongoing maintenance.
• A sound understanding of continuous improvement and right-first-time principles.
• The ability to translate quality requirements into practical, phase-appropriate solutions for a growing, early-stage organisation.
• A proactive, hands-on and collaborative approach, with the confidence to guide and support colleagues across functions.
• Strong problem-solving skills, sound judgement and a pragmatic mindset, combined with an unwavering commitment to compliance.

What we offer

• A high-impact role in an ambitious, innovation-driven biotech company.
• Direct involvement in pioneering therapies for unmet medical needs.
• A collaborative, agile and fast-paced environment.
• A role based in Antwerp, Belgium, with remote-working options tailored to your needs.
• Competitive salary and benefits.