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Details
Senior Quality Engineer
Reference: | JCAO1202 | Location: |
Dublin |
Qualification: | Degree | Experience: | 5-7 Years |
Job Type: | Permanent | Salary: | Not Disclosed |
May be suitable for:
Senior Quality Engineer
Senior Quality Engineer
Our client a high potential medical device start up is currently seeking a Senior Quality Engineer to join their team. The Senior Quality Engineer will report to the QA Manager and work across all stages of development, from prototyping, final manufacture, clinical investigation and commercialisation. The Senior Quality Engineer will support the QA Manager with maintaining the Quality Management System.
The Senior Quality Engineer should have a hands-on approach to projects with a motivated attitude and strong work ethic. An ability to work in a flexible and small entrepreneurial environment is essential.
Role/Responsibilities:
- Development of quality plans, programs and procedures, through all aspects of the product development process
- Ensure all work is carried out in compliance with Quality, Regulatory and company policies and systems.
- Ensure that performance and product quality conforms to company, customer and regulatory requirements.
- Review, analyse and report on quality discrepancies related to product design and manufacture
- Liaise and support OEM contractors/vendors during the manufacture of components and the assembly of devices for the purposes of design verification testing and clinical evaluation.
- Provide quality input and support for product development teams.
- Support the QA Manager in regulatory agency audits including FDA and Notified Body and aid in the preparation of non-conformity responses, as necessary.
Skills/Experience:
- Bachelor’s degree in a relevant Engineering or Science field
- 4-5 Years’ experience in medical device industry or equivalent higher-level postgraduate study (masters or PhD)
- Project planning, communication and writing skills
- Sound understanding of engineering fundamentals
- Medical device materials knowledge
- Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820) essential
For further information please contact James Cassidy [email protected] or call in confidence 0860204322
Quality Control Academic IT Biotechnology Project Manager Pharmaceutical Scientific Clinical Research Life Science Sales and Marketing Medical Device Connected Health Chemistry Supply Chain Pharma Sales Dublin Academic Quality Engineering Limerick Manufacturing Executive Biopharmaceutical Medical Affairs Allied Healthcare Laboratory Scientist Diagnostics Microbiology Cork City Mayo Sales and Marketing PhD Validation Engineer Supply Chain Quality Assurance Packaging Engineer Engineering Scientist Product Development Engineer Cork
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Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
This site uses cookies. More information on cookies can be found in our Privacy Policy | Terms of Use | Registered as a private limited company. No: 445328
Valid XHTML - CSS