Quality Auditor I (GMP / Pharma-Biotech)

Our client is an established organisation within the pharmaceutical/biotech sector, operating in a regulated GMP environment. They are focused on quality, compliance, and continuous improvement, with strong standards for documentation and patient safety. We are looking for a Quality Auditor (GMP / Pharma-Biotech) to support day-to-day quality activities on site. This role is ideal for someone with a solid GMP background who is comfortable managing deviations and CAPA processes, supporting investigations, and ensuring documentation meets regulatory expectations.

The successful candidate will work in both Dutch and English.

Responsibilities: Support the handling and follow-up of deviations, including documentation, tracking, and closure; Coordinate and support CAPA activities, ensuring actions are effective and completed on time; Participate in root cause investigations and help drive corrective and preventive measures; Support validation and qualification activities in line with GMP requirements; Perform document review to ensure accuracy, completeness, and compliance with internal and regulatory standards; Collaborate with cross-functional teams to maintain quality standards across operations; Contribute to continuous improvement initiatives within Quality Assurance.

Requirements: Strong working knowledge of GMP within a pharmaceutical or biotech environment; Hands-on experience with deviations, CAPA, and root cause investigations; Experience with validation/qualification and document review; Good command of Dutch and English (written and spoken); Able to work accurately in a highly regulated setting and manage multiple quality topics in parallel.

Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.