Description
Scientist - Downstream Process Development - NOVJP (m/f)
Reference: -en
Start: asap
Duration: 6 MM++
Main tasks:
- Responsible for the development and scale-up of protein pharmaceuticals (e.g. chromatography, filtration and ultrafiltration)
- Generate and review process transfer documents, manufacturing master batch records, consolidated batch records and campaign experience reports
- Generate or update source documentation to support regulatory filings worldwide, making sure that requirements of data integrity are fulfilled
- Work directly with CMC teams under minimal guidance by senior project experts
- Managing documentation related to GMP
Main qualifications
- M. Sc. or equivalent education in Biochemistry, Biochemical Engineering or a related discipline
- Experience in downstream process development and/or engineering
- Familiarity with GMP drug substance manufacturing requirements
- Fluency in English required and German would be advantageous
Main advantages:
- A city with a high quality of life that perfectly embraces both modern and traditional values
- You will work in an international environment
- A very renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
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