| Position | Device Quality Specialist |
| Posted | 11 Aug 2026 |
| Expired | 10 Sep 2026 |
| Company | Life Science Consultants |
| Location | Dublin | IE |
| Job Type | Full Time |
Latest job information from Life Science Consultants for the position of Device Quality Specialist. If the Device Quality Specialist vacancy in Dublin matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.
Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Life Science Consultants for the position of Device Quality Specialist below matches your qualifications.
LSC have a great contract opportunity for a Device Quality Specialist to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra-rare disorders through the innovation, development and commercialization of life-transforming therapeutic products. If you have 4+ years of experience working in the pharmaceutical, medical device, or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Support the Medical Device Quality Team in managing combination product quality records and document management activities. Support change control, CAPA, deviation, and Quality Management System (QMS) processes. Coordinate quality governance activities, audits, inspections, and management review reporting. Ensure quality records are processed and maintained in compliance with company procedures and regulatory requirements. Partner with cross-functional teams and external suppliers to support combination product quality and compliance. Support continuous improvement of the combination product Quality Management System. ABOUT YOU - ARE YOUR SKILLS A MATCH? Bachelor's degree or equivalent experience in a regulated industry. 4+ years' cGMP experience within Quality in a medical device, combination product, or pharmaceutical environment. Experience with Quality Management Systems, CAPA, Change Control, electronic QMS/document management systems (e.g. Veeva Vault), and medical device regulations including ISO 13485 and FDA 21 CFR Part 820. Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply! Apply via this advert or contact Jenny Murphy at LSC on if you have any more questions about this role! Skills: Quality Assurance Quality Systems Medical Device Change Control TPBN1_IJ
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