Job Description:
We are seeking a skilled professional to join our Medical Device organization based in Limerick. This is an excellent opportunity for individuals who want to be part of a leading multinational company that excels in its industry.
Duties and Responsibilities:
* Provide support for validation activities associated with equipment, reagents, facilities, cleaning, test methods, and environment.
* Manage complexity and serve as a technical expert for the Validation process to ensure compliance.
* Resolve and manage technical operational problems within the area of expertise.
* Suggest and implement innovation and continuous improvement within the Validation process.
* Facilitate successful team behavior within Quality Systems and across functional areas.
* Manage relationships externally and internally.
* Build cross-functional and cross-departmental support, fostering overall effectiveness.
* Foster harmony within Quality Systems.
* Review and approve Validation Master Plans, Protocols, Summary Reports, and other documentation associated with validations.
* Ensure all validation activities and documents are authorized and comply with regulatory requirements.
* Ensure timely completion of validation activities and assist in audits for compliance.
Education and Experience:
* Experience working in a regulated industry carrying out validations.