We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Limerick. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Duties

• Managing Complexity/Technical Accountability Serves as technical expert for the Validation process and responsibilities to ensure compliance
• Continuous Learning/Managing Risk Resolves & manages technical operational problems in area of expertise
• Suggest and sometimes may implement innovation and continuous improvement within the
• Validation process Implements initiatives in the Validation Process that will deliver customer value at lowest cost.
• Facilitates successful team behaviour within Quality Systems and across functional areas Manages relationships externally and internally.
• Builds cross functional and cross-departmental support, fostering overall effectiveness
• Fosters harmony within Quality Systems.
• Ensure accuracy and maintenance of the Validation Master List.
• Review and approve Validation Master Plans, Protocols, Summary
• Reports and other documentation associated with validations, as appropriate for each validation exercise.
• Ensure all validation activities and documents are authorised and appropriate compliance approval is gained.
• Ensure that all validation activities are carried out and reported in a timely manner.
• Ensure compliance through assisting in audits.