QA Officer
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
QA Officer supporting GMP compliance in Boxmeer, Noord-Brabant, pharmaceutical sector.
- Locatie
- Boxmeer, Noord-Brabant
- Werkvorm
- op locatie
- Uren
- 24–40 uur per week
- Contractvorm
- detachering
- Startdatum
- Eerste waarneming
- Opdrachtgever
- null
Eisen
- Hands-on experience with deviations, CAPA, and root cause investigations
- Strong GMP background within a pharmaceutical or biotech environment
- Fluent in Dutch and English (spoken and written)
- Experience with validation/qualification and document review
Omschrijving
Company: Our client is a well-established organisation within the pharmaceutical/biotech sector, operating in a highly regulated environment. They focus on quality, compliance, and patient safety, with robust processes and clear standards across their manufacturing and quality systems. Role Description: We are looking for a QA Officer to support the Quality Assurance team with day-to-day GMP compliance activities. This role is ideal for someone with a solid GMP foundation who is confident working on deviations, CAPA, investigations, and documentation review in a pharmaceutical or biotech setting. Responsibilities: - Supporting GMP compliance activities across the site, ensuring quality standards are met consistently - Handling and documenting deviations, including follow-up actions and on-time closure - Supporting CAPA processes, including tracking, documentation and effectiveness checks - Contributing to root cause investigations and helping drive corrective and preventive actions - Supporting validation/qualification activities by reviewing and managing related documentation - Performing document review to ensure completeness, accuracy, and compliance with internal procedures and GMP expectations - Communicating clearly with internal stakeholders in both Dutch and English to keep quality topics moving forward. Requirements: - Strong GMP background within a pharmaceutical or biotech environment - Hands-on experience with deviations, CAPA, and root cause investigations - Experience with validation/qualification and document review - Fluent in Dutch and English (spoken and written). Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me. Job ref: 58695. Start date: 8/13/2026.
Alle opdrachtenBekijk en reageer bij SIRE Life Sciences B.V. (externe link)
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