Quality Engineer
Brightwater
- Sligo
- €50,000 per year
- Permanent
- Full-time
- Provide Quality support to project manager, design engineers, production manager and clients.
- Establish compliant product specifications.
- Quality review of validation plan, company reports and protocols.
- Co-ordinate compliant product risk management files.
- Issue and review manufacturing records.
- Co-ordinate and review of testing and release of sterile product.
- Quality review of SOP'S.
- Review and approve of product change controls.
- Advise on quality related issues with clients.
- Perform CAPA reports.
- Conduct internal audits.
- Minimum level 8 degree in Science or Engineering discipline.
- 3-5 years medical device experience.
- ISO 13485 knowledge.
- Internal & external auditing experience.
- Validation experience (Sterilization, packaging)
- Ability to work on own initiative.
- Demonstrate detailed working knowledge of medical device environment.
- Excellent communication skills.
- Strong competitive salary
- Occupational Company Pension Scheme
- Health Insurance
- Continued Professional Development Support
- Educational Assistance
- Annual Leave service increment
- Subsidised Sport & Social Club
- Bi-annual Company events
- Employee Well being Programme of Events
- Flexible Working Policy (includes the option to apply for Flexi-Time, Flexible Working Hours and Remote Working)
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