Overview We are seeking an experienced CQV Engineer to support technical projects within a highly regulated pharmaceutical manufacturing environment. Reporting to the Senior Manager Validation & Compliance within the Site Engineering organization, you will play a
o you want to be part of a world wide organization recognized as Worlds Best Workplace with the mission of saving patients through advanced biotech technologies? Our clients products reach over 10 million patients worldwide, that
Commissioning, Qualification & Validation (CQV) Engineer (GMP) Location: Breda (On-site, 5 days/week) Contract Duration: 12 months (extension possible) Start Date: September (ASAP, max. 1-month notice period) Overview We are looking for a CQV Engineer (GMP) to