Regulatory Affairs specialist

Our customers are in more or less constant need of skilled and experienced RA consultants and we are therefore currently looking for persons who can take commit to a longer or shorter assignment at some of our customer for a longer or shorter period of time.

If you have experience from medical device and used to performing regulatory assessments,, creating regulatory strategies and plans for new developments - we would like to talk immediately! Especially of you have profound knowledge and experience in working within Medical device.

Experience from notifying bodies i e FDA is an advantage.

Who are you?

As a person you are:

- Selfsufficient and independent

- a teamplayer with integrity and ability build professional relationships with different stakeholders both internally and externally

- comfortable in your role as a consultant

- you have adeep and profound understanding of Regulatory affairs issues within Medical device

- you have an international approach to your work

What you can expect

Technogarden is a well established company with a growing Life Science business, you will have extensive support and you choose yourself whether you would like to work as a subcontractor within your won company or as employed if we get to cooperate.

You are most welcome to contact us as soon as possible so that we can tell you more about our assignments.