This is an exciting opportunity for an experiencedQuality Validation Engineerto join our client, aleading Life Science companybased in theirnew manufacturing facility inKilkenny. Responsibilities The development and maintenance of Quality System procedures. Ensuring the site delivers safe and effective products that meet customer needs whilst maintaining compliance. Monitoring and maintaining the quality and compliance status of associated quality records. Maintaining the quality and compliance status of associated Procedures, work instructions, and training materials. Presenting and communicating status, report metrics, identifying trends, potential issues, improvement initiatives, as applicable. The review and approval of validation documentation in accordance with divisional policies. Basic understanding of design controls and design transfer. Education And Experience Relevant third level qualification. Engineering/Manufacturing/Science is preferred. Minimum 2 years in the Engineering/Manufacturing/ Scientific field. Experience working in a 21CFR820 and/or ISO13485 regulated industry. May consider experience in pharmaceutical validations. Whats on Offer Attractive compensation package that includes competitive pay, as well as benefits such as Family health insurance, Excellent pension scheme Life assurance Career Development Fantastic new facility Growing business plus access to many more benefits. For a confidential discussionandmore information on the role,please contactKevin Griffin Kevin Griffin Skills: Validation Engineering Design Transfer