We are seeking an exceptional professional to join our team at {company}, a leading Medical Device organization based in Limerick. This is an exciting opportunity for anyone who wishes to collaborate with a multinational that consistently excels in its field.
The successful candidate will be responsible for providing support and guidance on the validation activities associated with equipment, reagents, facilities, cleaning, test methods, and environment. Key responsibilities include:
1. Providing technical expertise to ensure compliance with validation processes.
2. Managing complexity and resolving technical operational problems within the Validation process.
3. Suggesting and implementing innovation and continuous improvement within the Validation process.
4. Facilitating successful team behavior within Quality Systems and across functional areas.
5. Building cross-functional and cross-departmental support to foster overall effectiveness.
6. Fostering harmony within Quality Systems.
7. Reviewing and approving Validation Master Plans, Protocols, Summary Reports, and other documentation associated with validations.
8. Ensuring all validation activities and documents are authorized and appropriate compliance approval is gained.
9. Coordinating and reporting validation activities in a timely manner and assisting in audits for compliance.
To be considered for this role, candidates should have experience working in a regulated industry carrying out validations. If you are a highly motivated individual looking to contribute your skills and expertise to a dynamic organization, we encourage you to apply.