CQV Engineer

CQV / CSV / Validation Engineer – GMP Manufacturing

Contract: 3-4 months initially | Extension possible

Start: Immediate

I’m supporting a GMP-regulated manufacturing site just outside Zurich that requires additional CQV, CSV and validation engineering support during a period of increased project activity.

This role is suitable for engineers working across commissioning, qualification, validation and computer system validation, within regulated GMP environments.

Role overview

You’ll support site engineering, quality and validation teams with activities across equipment, processes and systems, helping ensure operations remain compliant and validated.

Key responsibilities

• Supporting commissioning and equipment handover activities
• Executing and supporting IQ / OQ activities
• Supporting PQ, process or cleaning validation where required
• Supporting CSV activities for regulated systems where applicable
• Preparing and reviewing GMP, CQV and CSV documentation
• Supporting deviations, change controls and validation lifecycle activities
• Working collaboratively with engineering, QA, IT and operations teams
• Experience in CQV, CSV or validation within GMP manufacturing
• Exposure to equipment, process or system validation
• Familiarity with regulated documentation and compliance requirements
• Comfortable working on-site in a contractor capacity
• Experience with in pharmaceuticals, biotech, medical devices or CMOs

Languages

• German preferred (Minimum B1-B2)
• Immediate start
• Initial 3-4 month contract with potential extension
• Fast, technically focused interview process

If you’re a CQV, CSV or validation engineer available for an on-site contract within a GMP environment, I’d be keen to speak.

Apply directly or message me for a confidential discussion.