Scientist stability studies
Stability Scientist (Analytical Development)
Product stability team focuses on the design, execution and evaluation of stability profiles of novel vaccines. The group supports the clinical development stages of the vaccines platforms and generates data that is used in preparation for future commercialization.
The Scientist will be a key player in the management of the various stability studies of the novel vaccines during the clinical development. He/she will work in a multidisciplinary environment and have a focus on preparation of stability protocols, stability reports, supporting documentation for IND/CTA filing, supporting shelf-life strategies, design of the stabilities studies, evaluation of the data and coordination of scientific investigations.
Since different CMC projects are carried out in teams comprising members from different departments, teamwork and flexibility are two very important characteristics that are required attributes. We offer a challenging position which allows you to work in a dynamic and international environment, ensuring diversity in your work and creating plenty of opportunities for personal development.
* Msc or Ph.D. Degree in Biochemistry, Pharmacy, or equivalent life sciences degree
* A minimum of 2-3 years pharmaceutical industry experience working under GMP standards.
* Experience with stability studies (design, reporting, ICH requirements) * Experience with analytical methods qualification and validation
* Knowledge of statistical analyses and data trending
Competences: The candidate fit for the job is independent, flexible, motivated and enjoys working in a team. Excellent organizational and communication skills, and a strong scientific mindset are key for this position
If you are interested in this position, please send me an email with your most recent resume + cover letter to: t.maas(@)progressiverecruitment.com