Doel van de functie
Maintaining the Quality Management System, preparing, reviewing and approving quality related documentation and providing QA support.
Omschrijving van werkzaamheden
- Maintaining the Quality Management System, including, but not limited to:
- Documentation control (review, update)
- Training registration
- Conducting QA activities including revision of QAAs, translation of documents (Dutch-English or vice versa)
Kennis en ervaring
- Minimum Bachelor degree in relevant field (e.g. pharmacy, chemistry, biology, life sciences).
- 1 year experience in pharmaceutical or medical device industry.
- Relevant experience in GMP production/ QA environment within a pharmaceutical company.
- Familiar with cGMP and sterile manufacturing.
- Proficient with MS Office (Outlook, Word, Excel, Powerpoint). Preferred knowledge of SAP, Trackwise and Veeva
Competenties
- Quality-Focused, attentive to detail and results-oriented.
- Ability to communicate effectively in Dutch and English (both written and oral).
- Ability to work independently in fast-paced environment with little supervision.