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
1. Provide support for the validation activities associated with equipment, reagents, facilities, cleaning, test methods, and environment.
2. Manage complexity and serve as a technical expert for the Validation process to ensure compliance.
3. Resolve and manage technical operational problems in area of expertise.
4. Suggest and implement innovation and continuous improvement within the Validation process.
5. Facilitate successful team behavior within Quality Systems and across functional areas.
6. Manage relationships externally and internally.
7. Build cross-functional and cross-departmental support, fostering overall effectiveness.
8. Foster harmony within Quality Systems.
9. Review and approve Validation Master Plans, Protocols, Summary Reports, and other documentation associated with validations.
10. Ensure all validation activities and documents are authorized and appropriate compliance approval is gained.
11. Ensure that all validation activities are carried out and reported in a timely manner and assist in audits for compliance.
Education & Experience
1. Experience working in a regulated industry carrying out validations.
If interested in this posting, please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.
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