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

• Provide support for the validation activities associated with equipment, reagents, facilities, cleaning, test methods, and environment
• 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.
• 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.

• Experience working in a regulated industry carrying out validations.