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.
58695
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Kalyan Raj
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