Get a reply from this employer — a resume and cover letter tailored to exactly what they’re hiring for.
CQV Engineers / CQV Consultants across Europe to support commissioning, qualification and validation activities for GMP-regulated facilities, equipment, utilities, systems and processes.
You will work closely with project, quality, engineering and operations teams during all stages of CQV projects across multiple countries, providing rigorous validation support for diverse pharmaceutical environments.
Locations: Across Europe (Ireland, UK, Netherlands, Belgium, Germany, Switzerland, Spain, France, Italy, Denmark and more) Contract & Permanent Opportunities Available soon.
We are building a network of experienced CQV professionals across Europe to support current and future projects within the Pharmaceutical, Biotechnology and Medical Device sectors.
As a CQV professional, you will support commissioning, qualification and validation activities for GMP-regulated facilities, equipment, utilities, systems and processes. You will work closely with project, quality, engineering and operations teams during