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Design Control Specialist

Technolution



Does developing documentation for medical devices sound like the right opportunity for you?

As a Design Control Specialist at Technolutions you will be part of a team of more than 10 skilled and enthusiastic colleagues working with development of medical devices. If you thrive in an outgoing, hands-on role, please read on.

We can offer you a challenging and developing job
Together with your colleagues you will work with clients ranging from start-ups to leading companies within the medtech and pharma industry and get the opportunity to work on a wide range of medical devices.

In your role you will typically be part of developing:

  • Design and Development Plan
  • Design and Development Plan Matrix
  • Design Input Requirements
  • Design Verification Planning and documentation
  • Design Transfer activities

We thrive on the synergy of our combined knowledge. To ensure optimal utilization and continuous improvement, we actively share and collaborate with each other within and across areas of competence.

We have a few wishes too
You have hands-on experience and enjoy the world of design control. You have knowledge within ISO 13485, ISO 14971, IEC 62366-1 and preferably also FDA requirements for development of medical devices.

You have a holistic approach to the development process to find solutions and give advice that takes our clients context into consideration.

You thrive working with highly qualified teams on diverse projects and find it natural to build good relations with clients and colleagues, because you know that creates the best conditions for delivering great results.

If you are ready to embark on a journey of innovation, then join our team of dedicated Design Control Specialists, where your expertise will shape the future of medical device development. Don't miss out on the chance to be part of a dynamic and supportive environment that empowers you to make a real impact.

Department: Design Control

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Technolution

Lyngsø Alle 3B, 2970 Hørsholm

With strong competencies in R&D combined with regulatory, quality- and project management we solve complex and challenging tasks within Pharma and MedTech.

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