Validation Engineer

This is an exciting opportunity for a Validation Engineer to join a leading multinational pharmaceutical company based in Cork. You will provide validation and technical support to the Vaccines IPT team, focusing on cleaning cycle development and cleaning validation.
Key Responsibilities: Execute cleaning cycle development, validation, and equipment PQ.Develop validation strategies, write protocols, coordinate with vendors, and prepare technical reports.Perform equipment and cleaning periodic reviews, CAPAs, deviations, and risk assessments.Support commissioning by reviewing and approving documents.Participate in cross-functional problem-solving teams for troubleshooting.Ensure adherence to regulatory guidelines, site EHS policy, and cGMP standards.Serve as a subject matter expert during regulatory inspections.Contribute to site audits, risk assessments, and QMS compliance activities.Qualifications: Bachelor's degree in Chemical Engineering, Biochemistry, Microbiology, Chemistry, or a related field.3-5 years of validation experience in a pharmaceutical or regulated environment.Proficiency in at least three of the following: C&Q validation, Cleaning Validation, Equipment Validation, Process Operations, or Process Engineering.Working knowledge of GxP systems (e.g., GLIMS, eVAL, electronic batch records) is advantageous.For a confidential discussionandmore information on the role,please contactKevin Griffin Kevin Griffin
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