Regulatory Affairs Manager (m/f/d)
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
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