Regulatory Affair Specialist - Denmark - Parallel Imports

If you are someone who enjoys working with Regulatory Affairs working on preparations, maintenance and the quality of products packaging then this could be for you. I am currently working with a client who is looking for someone who is interested in start a position as a Regulatory affair Specialist, working in the field and be a direct part of the processes of packaging and documenting of the quality of the processes. The company is importing both human and veterinary drugs. The parallel import that the company is working on will give you the opportunity to broaden your experience and knowledge of working with Regulatory Affairs. This will benefit you for future applications and career progression.

Another great opportunity working for this company is that they are still growing. This means that the company will be taking on more products and the work that you will be doing will continue to differ and increase your knowledge. To you this means that you will never be board. Also, because you are working with this you will be able to grow and progress your career. Giving you the chance to grow and develop alongside with the company. This will make you feel more involved and a part of the company and that your influence has an impact on the company.

Requirements:
* A life science background
* Experience in Regulatory Affairs
* Working with packing, applications and updated.
* Speaks Danish.

If this is something that sounds interesting to you and would like to hear more about this, then do not hesitate to call me Maren Asheim on +46 580927950 or send me an email with your CV in word format to M.Asheim@nonstop-recruitment.com.