Quality Officer

Agomab; Antwerpen; Hybrid; EUR 60,000 - 80,000; Full time

Benefits offered by this job

High impact role

Pioneering therapies in biotech

Collaborative environment

Antwerp-based with remote options

Competitive compensation

Job summary

Agomab is seeking a Quality Officer to join the growing Quality team in Antwerp. You will help maintain and improve the QMS, own document control, and provide practical quality support across the organisation.

In this hands-on role, you will work under the Head of Quality to ensure GMP/GCP compliance, lead internal audits, and support regulatory inspections in a dynamic early-stage biotech environment.

Qualifications

• Bachelor's degree in life sciences or related field is required.
• Minimum of three years' experience in quality within biotech/pharma settings.
• Demonstrated GMP/GCP quality system knowledge with recent training or certification.
• Hands-on experience with electronic quality management systems and maintenance.
• Strong continuous improvement mindset and right-first-time principles.
• Ability to translate quality requirements into practical solutions for a growing biotech.

Responsibilities

• Act as a key Quality contact across Agomab and guide colleagues.
• Support development and maintenance of the QMS including procedures and training.
• Coordinate document control and approve operational documents.
• Facilitate risk management, CAPAs, and change control.
• Plan and conduct internal audits and support external audits.
• Prepare and follow up on management review meetings.
• Support validation and lifecycle management of electronic systems.
• Champion continuous improvement and compliance culture.

Skills

GMP/GCP knowledge

Quality management

Documentation control

Problem solving

Cross-functional collaboration

Education

Bachelor's degree in life sciences

Tools

Electronic QMS

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.