Quality Engineer
Cpl Group
- Galway
- Temporary
- Full-time
- Responsible for displaying professional behaviour with both internal and external business associates that reflects favourably on the company and is consistent with the company's policies and practises.
- The obligation to comprehend and uphold knowledge of the potential negative effects of performing their profession incorrectly.
- Completes challenging assignments by possessing and using extensive understanding of Quality and its application to the realm of post-market surveillance.
- Acquires in-depth knowledge of global operations and structures to make wise judgements and give guidance to the BU Quality and Regulatory teams and other functional areas.
- Delivering initiatives on behalf of the Division and with the assistance of the Business Units is your responsibility.
- Drives cross-functional compliance in coordination with the divisional for teamwork and multi-site conformance to pertinent regulatory standards.
- Provide resolutions with the best possible outcome in ambiguous circumstances and occasionally with incomplete information, agreement is sought. utilises risk assessment procedures under these conditions.
- Carry out any additional tasks or projects that are given to you.
- 3rd level qualification science or a related discipline.
- 3 years' experience in the medical device industry, specifically in a regulated environment. For example, CE, FDA, PAL, IVDR, MDSAP.
- Experience in development of medical devises, desirable.
- Proficient in MS Suite.