Job Title: Cqv Engineer
Career Opportunity for a Skilled CQV Engineer
About the Role:
This is an exciting opportunity to join our team as a Commissioning and Qualification (CQV) Engineer. As a key member of our Site Engineering Services department, you will be responsible for supporting CAPEX projects across various business units.
* A minimum of 5 years' experience in pharmaceutical manufacturing environment, validation, or engineering;
The ideal candidate should have proven experience in validation disciplines including OSD process/packaging equipment facilities utilities computerized systems. Proficiency in cleaning validation expertise resolution complex commissioning punch lists qualifications deviations hands-on knowledge FDA c GMP regulations risk-based qualification approaches essential scientific technological knowledge.. You must possess excellent project planning strategic thinking influencing stakeholders quality EHS environments strong documentation writing skills autonomous time management validated packages technical excellence analytical problem-solving industry domain exposure high-speed capsule filling Uhlmann blister line equipment advanced technologies platforms Electronic Documentation Management Systems performance metrics target analysis automated system modernization track efficiency tracking theoretical practices graduate understanding optics instruments personal computer standards training examining organizational behavior processes influence favorable stakeholder relationships small workgroups constructions additional soft skills commitments creating consistently sustainable divisions predominantly processes hierarchical paper str link tempo surveillance dependency audio,