Validation Engineer
Morgan McKinley Cork
We are looking for a Validation Engineer to join our client, a leading Biopharmaceutical company in Cork for a 6 month hourly rate contract. Client is targeting an early 2026 February start date.
Key Responsibilities- Project validation support including conducting equipment performance qualifications (specifically cleaning and sterilization validation)
- Authoring project validation master plans; SOP and documentation updates; Authoring validation protocols and final reports, executing validation studies, analysis of validation data; Resolving technical issues encountered during study execution.
- This individual will be required to work in a cross-functional team and independently to accomplish validation project objectives.
- Works with moderate work direction and is skilled and knowledgeable to the position.
- Degree in Engineering or a Scientific related discipline.
- Minimum of 3 years + experience working in a Validation role within Pharmaceuticals or Medical Device.
- Equipment Validation and Sterilization Validation experience.
- The successful candidate must have strong technical writing and oral communication skills.
Cork
Desired Skills: validation,quality assurance,medical devices
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