Job Opportunity with Award-Winning Medical Device Organization
We are seeking a skilled professional to join our team at an award-winning Medical Device organization based in Limerick.
This is an excellent opportunity for individuals who want to work with a leading multinational company that is renowned for its excellence in the industry.
Duties and Responsibilities:
* Provide support for validation activities related to 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 in area of expertise.
* Suggest and implement innovation and continuous improvement within the Validation process.
* Foster 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 appropriate compliance approval is gained.
* Ensure that all validation activities are carried out and reported in a timely manner and assist in audits for compliance.
Requirements:
* Experience working in a regulated industry carrying out validations.
About the Role:
This role offers an exciting opportunity for individuals who want to work with a leading multinational company that values innovation, collaboration, and excellence. The ideal candidate will have a strong background in validation and quality systems, with excellent communication and problem-solving skills.