A Quality Engineer/ CAPA Coordinator is required for a Staff position with a leading Medical Device Contract Manufacturer based in Cork. The Cork facility is a global strategic expert in the automated production of medium-high volume complex and disposable medical devices. The facility has been in operation for over 30 years. This is an opportunity to work in an ever changing and technologically advanced site.
In this role the CAPA Coordinator will be responsible for:
o Expert in the agile CAPA System (CCN, CAR, SCAR and PAR) and associated Processes.
o Review and help script CAPA in a Regulatory Compliant Manner
o Provide Training and Expertise in the CAPA Process
o Review, Evaluate, Verify and check the effectiveness of CAPA as required
The CAPA Coordinator requires:
o A Degree in Science or Engineering, or a lesser qualification with sufficient job related experience
o At least 4+ years Quality, Quality Assurance / Regulatory affairs experience in a similar Quality Engineering role in electronics manufacturing or Medical Devices Industries.
o Ideally experience of the CAPA Process in a regulated environment
If this role is of interest, please call Ruth at LSC on 021 4777 329 or apply directly through this advert.