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Job Details

Regulatory Affairs Specialist - Medical Device, Germany

Company: Barrington James Clinical
Reference: CRBG - SpecRA
Closing Date: 04 Mar 18
Type: Permanent
Salary (£): Competitive

Job Summary:

For more information call Carlos Biggemann on +44(0)1294 776644 or email


Main Purpose of Job:

The Regulatory Specialist EMEA is responsible for preparation, maintenance of registration files as well as for executing tasks related to the administrative processes of product registrations.

Key Duties & Responsibilities:

  • Under direction of the supervisor compile and maintain registration files for countries in EMEA.
  • Support in timely registration of new products and maintenance of registered product license in countries assigned by the supervisor.
  • Execute administrative tasks related to the product registration process
  • Support the business in obtaining on-time documents required to import/export products or to obtain reimbursement
  • Communicate with consultants, agents, distributors or other stakeholders in relation to registrations in process.
  • Other activities as needed assigned by the supervisor in support of regulatory processes and/or registrations

Essential Experience/Skills:


Preferably a Bachelor (Hochschule) or University Degree in Science, Engineering, and/or Biotechnology or equivalent relevant experience


Minimum 2-year experience in Regulatory Affairs in Medical Device/Pharmaceutical industry in EMEA, preferably in a multi-cultural environment.

Skills/ Knowledge/ Ability:

  • Experience with handling regulatory files and submission processes
  • Excellent interpersonal and communication skills
  • Able to work independently
  • Meticulous and attention to details.
  • Good English communication skills verbally and in writing


Apply for this job: Regulatory Affairs Specialist - Medical Device, Germany

Contact Information:

Address:  Head Office
Victoria House Consort Way Horley Surrey
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

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