Quality Officer
Il y a 17 heures
Antwerp, Belgique
Agomab
Temps plein
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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.
- 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.