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Job Description
Validation Engineer: Develop and execute validation strategies for a leading biologics client based in Cork, ensuring compliance with regulatory guidelines and highest standards for quality, safety, and compliance.
We are seeking a skilled Validation Engineer to join our team. The ideal candidate will have 3-5 years of experience in a validation specialist role in a pharmaceutical or highly regulated environment. Responsibilities include: * Executing cleaning cycle development, cleaning validation, and process validation * Writing and adhering to validation strategies, coordinating with vendors, and preparing technical reports * Providing technical support during commissioning and ensuring documentation complies with standards * Participating in cross-functional problem-solving teams and providing technical input during regulatory inspections * Ensuring compliance with site EHS policy, cGMP, and other business regulations Requirements: * 3-5 years' experience as a validation specialist in a pharmaceutical or highly regulated environment * Bachelor's degree in Chemical Engineering, Biochemistry, Microbiology, Chemistry, or a related field * Experience in at least three of the following areas: C&Q validation, Cleaning Validation, Equipment validation, Process operations, or manufacturing, Process Engineering * Working knowledge of GxP systems, including GLIMS and eVAL, electronic batch records This is a contract position with an initial 11-month term. The successful candidate will report to the Vaccines IPT Associate Director and work closely with the Vaccines IPT team.