QA/RA Specialists - Medical Devices
Location - Ballymena
Industry - Growing Healthcare Company
Do you want to play a key role in ensuring compliance with CE, FDA, and international standards, managing audits, maintaining QMS (ISO 13485:2016), and supporting product registrations?
You'll also liaise with suppliers, lead post-market surveillance activities, and maintain technical files.
What You'll Need:
* Degree in Engineering, Biological Sciences, or relevant experience
* Strong knowledge of ISO 13485:2016, ISO 14971, MDR, IVDR
* Experience in QA/RA roles within medical or IVD device sectors
* Proven ability to compile and manage CE technical files
This is a fantastic opportunity to join a company at the forefront of medical innovation during an exciting growth phase.
Apply now to take your QA/RA career to the next level!
To speak in absolute confidence about this opportunity please send an up to date CV via the link provided or contact Kathy Donaghey Specialist Consultant at MCS Group 028 96935521
Even if this position is not right for you, we may have others that are. Please visit MCS Group to view a wide selection of our current jobs www.mcsgroup.jobs
Not all agencies are the same…MCS Group are passionate about providing a first-class service to all our customers and have an independent review rating of 4.9 stars on Google
#J-18808-Ljbffr