Morgan McKinley is partnering with a leading Cork based medical device manufacturer who is seeking a Quality Engineer for an hourly rate long term contact.
The successful candidate will have a proven track record supporting quality in a manufacturing setting. They will have over 2 years experience as the quality engineer managing Non conformances, CAPA's and all quality issues relating to production. This individual will be self-driven and passionate about representing quality to the highest standards.
Required;
- Minimum of bachelors of science degrees in manufacturing / engineering
- 4+ years experience in a manufacturing environment or equivalent with direction experience in a Quality environment (preferable GMP regulated)
- Experience in the Medical device industry is a distinct advantage. Else, in a highly regulated automated environment.
The Role;
- Drive and implement process improvements to ensure predictable processes across all product lines, including risk reduction, yield improvement, error proofing, cost reduction initiatives and process automation activities.
- Provide effective and response QA support to operations to meet their areas objective of quality cost and output.
- Immediately respond to non-conformances, process deviations, and line-down situations to implement effective, rapid containment actions and minimize impact on production schedules.
- Lead and execute in-depth investigations into quality issues using structured problem-solving methodologies to identify and document the true root cause of failures.
- Drive and implement plant wide quality systems improvements
- Management of incoming inspection area to ensure efficient supply to production areas
If you are keen to further develop your career with a leading Medical Device company while working with a highly collaborative team please reach out today to hear more about this exciting opportunity. For more information please contact Orla Casey 021 230 0497
