# Quality Officer at Agomab

> Hybrid · Belgium · Unspecified · Other · open. Source: https://alderhq.app/jobs/pinpoint%3Aagomab%3A608298 (read 2026-11-08).

## Facts (observed)

- Company: [Agomab](https://alderhq.app/companies/agomab)
- Location text: Agomab Antwerp, Antwerp
- Where it can be done from (inferred): Hybrid · Belgium (evidence: "Location: Agomab Antwerp, Antwerp")
- Posted: already open when tracking began; date unknown
- First seen by alder: 2026-11-04 · last verified: 2026-11-04
- Reposted: 0 times · edited: 0 times
- Apply on the employer's site: https://agomab.pinpointhq.com/en/postings/e0cca6a4-bdb5-45ff-a85a-b298d31f80e4
- Skills listed (inferred): GCP

## Pay and sponsorship

- Posted pay: not posted

## Description (the employer's text)

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.

### 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

- 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.
### Benefits

- 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.

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Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/pinpoint%3Aagomab%3A608298 and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.