Quality Project Associate
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Join a leading team providing essential quality oversight and project support within the pharmaceutical industry. This role offers you the chance to contribute significantly to quality assurance processes and product launches in a state‑of‑the‑art aseptic manufacturing environment.
As the ideal candidate, you are a driven Quality Project Associate ready to ensure compliance and facilitate successful project executions. Your attention to detail and strong analytical skills will be essential in this pivotal position.
- You perform quality reviews of validation documentation, change records, and procedures.
- You coordinate regulatory submissions with precision.
- You provide support for Quality Management Systems, including validation, Quality Risk Management (QRM), and change management.
- You conduct end-to-end validations of new products, preparing validation documents and analyzing results.
- You support the creation and maintenance of Master Batch Records.
- You actively contribute to continuous improvement initiatives.
Requirements
- You hold a Master's degree in a relevant scientific or engineering discipline or possess equivalent experience in fields like Biochemistry or Biotechnology.
- You have a background in project management within the pharmaceutical industry, especially in GMP‑regulated and aseptic environments.
- You possess strong analytical and problem‑solving abilities.
- You are an excellent organizer with a meticulous and quality‑conscious work approach.
- You demonstrate strong communication, interpersonal, and technical writing skills.
- You are proficient in Dutch and possess good knowledge of English (written and oral).
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