On Site Contract Compliance Jobs
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Senior CQV Engineer
Role Overview We are looking for a Senior CQV Engineer for a duration of 12 months, to support pharmaceutical manufacturing projects, with primary responsibility for commissioning and qualification of GMP manufacturing equipment. The role requires a hands-on engineering profile capable of independently driving CQV activities from planning and proto...
C&Q Engineer
We are seeking an experienced Commissioning & Qualification (C&Q) Engineer to support ongoing qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment. The successful candidate will play a key role in coordinating qualification documentation, executing qualification activities, and ensuring alignment b...
Metrology Engineer
Metrology Engineer: Medical Devices | Contract Opportunity | Cork, Ireland Location: Cork, IrelandContract Length: 1-2 YearsType: Full-time, 40 hours/ week A leading medical device manufacturer is seeking an experienced Metrology Engineer to join their team on an initial 1-2 year contract based in Cork, Ireland.This position will support manufactu...
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Senior Packaging Engineer
Senior Packaging Engineer (Contract)Location: Madrid, Spain Duration: Initial 6-12 Month Contract Industry: Medical Devices / Packaging Development Eligibility: Spanish or EU CitizensAbout the OpportunityWe are supporting a global Medical Device organisation in the growth of its Packaging Development function in Madrid. This team is responsible for...
Packaging Technician
Packaging Technician (Contract)Location: Madrid, Spain Duration: Initial 6-12 Month Contract Industry: Medical Devices / Packaging Development Eligibility: Spanish or EU CitizensAbout the OpportunityWe are supporting a global Medical Device organisation in the expansion of its Packaging Development function in Madrid. This team plays a critical rol...
Asset CQV Engineer
Asset Engineer (CQV) - Ghent, Belgium (Fully Onsite)OverviewWe are seeking an experienced Asset Engineer (Commissioning, Qualification & Validation) to join a leading pharmaceutical manufacturing facility in Ghent, Belgium. This position is responsible for ensuring manufacturing equipment, utilities, and systems remain qualified, compliant, and in ...