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Regulatory Affairs Manager (m / f / d)
GULP – experts unitedCologneVor 30+ Tagen
StellenbeschreibungPlanning, 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 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
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
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Manager Mfd • Cologne