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À propos
Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.
Apply now, read the job details by scrolling down Double check you have the necessary skills before sending an application.
This role will play a critical part in delivering validation activities across key projects, with a strong focus on equipment performance qualification, including cleaning and sterilisation processes.
Key Responsibilities- Lead planning and execution of Equipment/Engineering Performance Qualification (EMPQ) activities
- Develop Validation Master Plans and associated validation lifecycle documentation
- Author and execute validation protocols and comprehensive summary reports
- Analyse validation data and provide clear technical conclusions
- Update and improve SOPs and validation documentation as required
- Troubleshoot and resolve technical challenges during study execution
- Collaborate effectively within cross‑functional project teams while also operating independently
- Proven experience in EMPQ planning and execution within a regulated pharmaceutical manufacturing environment
- Strong technical writing skills with a high level of documentation xcfaprz accuracy
- Ability to work with minimal supervision and drive deliverables to completion
- Confident communicator with strong problem‑solving capability
This is an excellent opportunity for a validation professional who thrives in a dynamic, compliance‑driven manufacturing environment and can deliver high‑quality results with limited oversight.
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Compétences linguistiques
- English
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