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Manufacturing Process Engineer
Negotiable

Senior Additive Manufacturing Process Engineer (Contract) - 6months Our client is seeking a hands-on Senior Additive Manufacturing Process Engineer to support its growing 3D-printed titanium implant manufacturing operation. The consultant will investigate and reduce manufacturing non-conformance's across multiple additive manufacturing machines, wi...

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Senior Process Engineer (9 months)
Negotiable

We are seeking an experienced Senior Process Engineer to support a major pharmaceutical project based in Lombardy, Italy. This is an urgent requirement for a highly skilled engineering professional with a strong background in pharmaceutical process design and project execution. The successful candidate will play a key role in the engineering and de...

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CQV Consultant
LyonNegotiable

CQV Consultant (Contract)Location: Lyon Region, France (On-site) Contract Length: 12 Months Industry: Pharmaceuticals Start Date: ASAPThe OpportunityWe are supporting a leading pharmaceutical manufacturing site undergoing a significant capital investment and expansion programme. As part of this project, we are seeking an experienced CQV Consultant ...

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Selby Jennings Start Your Career In Recruitment
NPI Engineer
Negotiable

EPM Scientific are currently supporting a leading MedTech client to recruit 2 Project Engineers to join their Cork site on initial 18 month contracts, supporting Cleanroom NPI activities. Both roles are ASAP starts, primarily on site, and paid on a daily rate.Job description:Drive process development, optimization, and cost reduction initiatives ac...

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Process Validation Engineer
BarcelonaNegotiable

Validation Engineer / Process Validation Engineer (Injection Moulding)Location: Fraga, Spain Contract Length: 6-12 Months (Potential Extension) Hours: 40 Hours per Week Working Pattern: HybridOverviewWe are seeking an experienced Validation Engineer to support a high-volume programme of process validation activities within an injection moulding ma...

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Process Engineer
LyonNegotiable

Key ResponsibilitiesSupport and execute process and technology transfer activities for sterile drug products.Prepare, review, and author GMP-compliant technical documentation and transfer packages.Evaluate manufacturing processes, equipment suitability, process performance data, and facility readiness.Review deviations, investigations, CAPAs, proce...

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