RA/QA Specialist

Location Netherlands
Discipline: Medical Device
Job type: Permanent
Contact name: Christian Steenkamp

Contact email: c.steenkamp@panda-int.com
Job ref: 15697
Published: 27 days ago

At this moment, I am looking for a RA/QA Specialist to join a well-established global Medical Devices company aiming to accommodate new and evolving initiatives.

In this role you’ll be involved in the multi disciplinary projects, wherein you’ll frame/ plan the execution of the compliance processes together with the QA Manager. Next to that, you’ll be active with Risk Management, Project Management and support QA activities like maintaining the QMS.



  • Ensure that Regulatory processes are implemented and maintained in EMEA and defined within the projects in partnership with countries and (external) stakeholders
  • Manage and communicate progress of Regulatory projects and coordinate activities with departments like RA, Manufacturing, etc.
  • Develop, maintain and share appropriate documentation of processes and methods
  • Ensure establishment of all necessary infrastructure for compliance and implementation
  • ISO 13485 compliance of project activities
  • Support Medical Device QA activities like maintaining the QMS.



  • Bachelor or higher degree (or equivalent) in a relevant area like Life Sciences or Engineering
  • At least 3 years’ experience in QA/RA of Medical Device or Pharma (MDD/ MDR/ ISO13485)
  • Proven experience in Project Management
  • Excellent English verbal and written skills
  • Pro-active, strong communicator, open and transparent, self-starter and pragmatic.



With years of investigative insight, the company remains committed to the discovery, exploration, and development of ophthalmic therapies. Now, and into the future. Their clinical development network now spans three continents.

The organisation offers a competitive salary and benefits.


INTERESTED? Reach out to Christian Steenkamp for more information by contacting +31 (0)20 20 44 502 or c.steenkamp@panda-int.com