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.
What are we looking for?
* 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).