Job Description
Our client is seeking a skilledComputer Systems Validation Engineerwith experience in software change management and cybersecurity assessments. This role offers the opportunity to join a global medical device organization. Responsibilities The validation and operational management of computerized systems. The creation and review of validation documentation in accordance with regulatory requirements and divisional policies. Responsible for creating Software Compliance assessments such as 21 CFR Part 11 and Data Integrity. Maintaining the quality and compliance status of associated Procedures, and work instructions. Presenting and communicating status, reporting metrics, identifying trends potential issues, and improvement initiatives, as applicable. Qualifications and Experience Relevant third-level qualification. Engineering/Manufacturing/Science is preferred. 2-3 years of working knowledge of software validation in the medical devices industry. Experience working in a 21CFR820 and/or ISO13485-regulated industry. May consider the experience in pharmaceutical validations Benefits 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 Skills: Validation Engineering Software