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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