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Regulatory Affairs Consultant - 80% Home Based

  • Job type: Contract
  • Location: Warszawa
  • Salary: Competitive
  • Job reference: GDL4567
  • Sector: EPM Scientific, Regulatory
  • Date posted: 12/01/2018

A Multinational Medical Device company is looking for experienced Regulatory Affairs consultants to join their Warsaw-based project for a 6 month basis.

My client is looking for consultants that can aid the notification of their exciting new product in Slovenia and The Czech Republic. The company is looking to expand their presence in these territories with increased investment and expansion.


Responsibilities:

-          The notification of Medical Devices, Cosmetics, Batteries and Veterinary Medical Devices
-          Cooperate with the local distributors and supplier’ approval processes.
-          Tracing local Medical Device regulations with regard to the new MDR implementation.  


Experience and Skill Requirements:

-          Either Slovakian or Czech Fluency alongside English and Polish skills
-          Experience with Regulatory affairs in Pharma or Medical Device Industries
-          OR 2 years within Quality Assurance or Quality Control in Pharma or Medical Device industry


What this Job Offers You:

-          Flexibility to be home based with only one day a week onsite in Warsaw.
-          Secure 6-month contract.
-          Opportunity to work with a Multinational Medical Device company.

How to Apply:

Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact Enquires(@)epmscientific.com or phone +442037588865 .


 



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