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Validation Engineer - 12 months - 0.8 FTE
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Our Client, An established global medical manufacturing organisation is seeking a Validation Engineer to support new product introductions and the validation of manufacturing processes in a regulated environment.
Key Responsibilities
- Write & execute process validation protocols
- Support QMS improvements and compliance (ISO 13485 / ISO 14001)
- Lead risk assessments and change controls
- Support GMP audits, data analysis, and continuous improvement (Lean / Six Sigma)
- Perform root cause analysis and implement corrective actions
- Collaborate cross-functionally and with external vendors
Requirements
- Degree in Engineering, Polymer Science, or equivalent experience
- 2+ years’ experience in Medical Manufacturing
- Problem‑solving skills & good communication
How to apply
If you are interested in this opportunity, please send your CV and a short cover letter highlighting your relevant experience. xcfaprz Applications will be handled in confidence and reviewed on a rolling basis.
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Compétences linguistiques
- English
Avis aux utilisateurs
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