Scientist Analytical Development
Location: NetherlandsThe Company
They are a Biopharmaceutical company that specializes in the development of vaccines to cure infectious diseases worldwide.Role Description
Management of various stability studies of the novel vaccines during the clinical development. You will work in a multidisciplinary, dynamic and International environment.Responsibilities
- Preparation of stability protocols and reports- Documentation for IND/CTA filing
- Support of shel-life strategies
- Responsible for the design of stability studies
- Evaluating data and coordination of scientific investigations
Requirements
- MSc degree or higher in (Bio)chemistry, Pharmacy or related area- 2+ years of experience in a Biopharmaceutical environment and working with GMP
- Experience with stability studies, analytical methods, qualification and validation
- Understanding of statistical analyses and data trending
Other information
This is a fulltime job, 32 hours is discussable. The ideal candidate is independent, flexible, motivated and a teamplayer. Furthermore excellent skills in organizing, communication and someone with a scientific mindset and eye for detail.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Bram Reulen.
Opis stanowiska
The Company
They are a Biopharmaceutical company that specializes in the development of vaccines to cure infectious diseases worldwide.Role Description
Management of various stability studies of the novel vaccines during the clinical development. You will work in a multidisciplinary, dynamic and International environment.Responsibilities
- Preparation of stability protocols and reports- Documentation for IND/CTA filing
- Support of shel-life strategies
- Responsible for the design of stability studies
- Evaluating data and coordination of scientific investigations
Requirements
- MSc degree or higher in (Bio)chemistry, Pharmacy or related area- 2+ years of experience in a Biopharmaceutical environment and working with GMP
- Experience with stability studies, analytical methods, qualification and validation
- Understanding of statistical analyses and data trending
Other information
This is a fulltime job, 32 hours is discussable. The ideal candidate is independent, flexible, motivated and a teamplayer. Furthermore excellent skills in organizing, communication and someone with a scientific mindset and eye for detail.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Bram Reulen.
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Kontrola jakości / Audyt produkcji