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 key
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
Our client is looking for an experienced Project Manager with a strong technical background to lead complex equipment projects from concept through execution and final handover. In this role, you will manage multidisciplinary projects involving process equipment, manufacturing systems,
Company Description Movu Robotics Innovation, ambitious growth, technology, state-of-the-art robots – that’s Movu Robotics in a nutshell. Due to the in-house design and manufacturing process of our systems, an exciting, hands-on work environment with plenty of