Validation Engineer

Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.

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.

• 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.