Regulatory Affairs Manager (m/f/d)

GULP – experts united
Cologne
Diese Stelle ist in deinem Land nicht verfügbar.

If you are thinking about a new career start, then we should talk! We currently have an exciting vacancy for a Regulatory Affairs Specialist with a business partner in Cologne .

A variety of tasks, an appreciative working atmosphere and attractive benefits await you - all in a permanent position directly with the client from the pharmaceutical industry .

Sounds good? We look forward to receiving your online application. Equal opportunities are very important to us - applicants with a disability are very welcome!

Here's what our clients offer

  • Direct placement in attractive positions with reputable companies
  • Unique network with both large and medium-sized companies in the region
  • Appreciative and trusting support throughout the entire placement process
  • Intensive preparation for the interview with our client
  • Attractive, performance-related remuneration

Your tasks

  • Planning, organization and implementation of national procedures for new marketing authorizations, marketing authorization renewals and marketing authorization variations for medicinal products
  • Collaboration on corresponding European procedures (MRP, DCP, CP) for medicinal products in close cooperation with the European authorization team
  • Implementation of regulatory and safety-related requirements in the product texts of medicinal products
  • Acting as an interface to national authorities and employees in the Marketing, CMC, PV and Quality departments

Your profile

  • Completed scientific studies (university degree, e.g. in chemistry or biology), possibly also pharmacy or medicine
  • Several years of professional experience in the approval area of the pharmaceutical industry
  • Good knowledge of relevant legal regulations for medicinal products
  • Good knowledge of German
  • High motivation and an independent and goal-oriented way of working
  • Vor 30+ Tagen
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