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This job expired on 28/07/2026. It no longer accepts applications.
Quality Assurance Operations Specialist
Lonza · Verviers
Job description
About the role
The Quality Assurance Operations Specialist provides day‑to‑day support for all quality‑related operational activities at a manufacturing site. You will make quality decisions for both planned and unexpected events, applying a risk‑based mindset while collaborating closely with production teams.
Key responsibilities
- Release finished products after thorough review of quality documentation.
- Review and approve production records, including batch documentation and logs.
- Manage quality events such as deviations, investigations, CAPAs, and changes.
- Support production by resolving in‑process and shop‑floor quality issues.
- Review and approve pre‑production documentation using a risk‑based approach.
- Handle product complaints from registration through customer response.
- Act as the primary QA contact for stakeholders with quality‑related queries.
Required profile
- Degree in Chemistry, Biology, Microbiology, Pharmacy or a related field.
- Experience in QA or a similarly regulated environment.
- Strong understanding of GMP and quality standards.
- Ability to assess risk and make confident, timely decisions.
- Experience reviewing deviations, investigations, or quality events.
- Strong organisational skills and ability to manage multiple priorities.
- Effective communication skills and confidence working with cross‑functional teams.
Required skills
- Good Manufacturing Practice (GMP)
- Risk assessment
- Deviation management
- CAPA implementation
- Quality documentation review
- Batch record approval
What we offer
- Agile career and dynamic working culture.
- Inclusive and ethical workplace.
- Competitive compensation with performance‑based recognition.
- Relocation assistance for the successful candidate.
- Annual base salary range €47,250 – €66,150.
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Lonza
Verviers
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