Clinical Supply Chain QA Specialist

Opdrachtgever: Word lid of log in
Standplaats: Breda
Regio Brabant, Limburg, Zeeland
Duur opdracht in maanden: niet vermeld
Indicatie uurtarief: niet vermeld
Aantal uren per week: niet vermeld
Opleidingsniveau: Master / Universitair
Laatste update: 16 oktober 2026
Sector: Farmaceutische & Chemisch...

Sommige informatie en reageren zijn alleen beschikbaar voor ingelogde interim professionals.

Quality & Validation Management
  • Master's degree, ideally in Life Sciences or a comparable discipline
  • Multi-year background in Quality Assurance and/or manufacturing within the pharmaceutical, biotech or medical device sector
  • Hands-on experience with documentation review, such as batch records, and deviation/investigation support
  • Solid knowledge of GMP and GDP; GCP knowledge is a plus
  • Keen eye for detail, methodical approach and a compliance-driven mindset
  • Effective communication skills combined with the ability to work with various stakeholders
  • Fluent in English

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