Company
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.
Job Description
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.
58690
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Neetu Parkala
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