CQV Engineer
Listed on 2026-01-24
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Engineering
Pharma Engineer, Validation Engineer
Engineering / Qualification Contractor – Pharma Packaging & Serialization
Contract: 3-4 months initially | Extension possible
Start: Immediate
I’m supporting a pharma manufacturing site in Switzerland that requires an experienced engineering / qualification contractor to support a busy period tied to incoming packaging equipment and a live customer project.
This is a hands-on, site-based role suited to contractors who are comfortable operating autonomously in GMP environments and contributing across engineering, qualification and serialization activities.
What you’ll be doing- Supporting engineering activities for pharmaceutical packaging equipment
- Leading or supporting equipment qualification (IQ / OQ, some PQ exposure)
- Involvement in serialization and aggregation activities on packaging lines
- Supporting process validation post-qualification
- Producing and reviewing GMP documentation (SOPs, protocols, reports)
- Working closely with internal engineering teams and external customers (remote interaction)
- Engineering or CQV experience within GMP manufacturing
- Exposure to pharma packaging equipment qualification
- Serialization experience is a strong advantage (line-level, not IT-only)
- Comfortable working on-site as a contractor and taking ownership
- Experience with in CMOs / contract manufacturing beneficial but not essential
- German preferred
- Fast interview process (likely a single technical discussion)
- Approved and urgent requirement
- Junior-to-mid contractors considered if serialization exposure is present
- Senior contractors also welcome
If you’re a packaging, engineering or CQV contractor with exposure to serialization and are available for an on-site assignment in Switzerland
, I’d be keen to have a confidential discussion.
Apply directly or message me to discuss suitability.
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