Role DescriptionThe group supports the clinical development stages of the vaccines platforms and generates data that is used in preparation for future commercialization. The Coordinator will be a key player in the support of the various stability studies of the novel vaccines during the clinical development. 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.
ResponsibilitiesThe coordinator will work in a multidisciplinary environment and have a focus on preparation of various documents such as stability protocols, stability reports, amendments, shelf-life extensions. The person will support other Stability scientist in daily management of studies by preparation of data tables, evaluation and visualization of data trends and communication to relevant stakeholders. 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.
Requirements• BS or MS Degree in Biochemistry, Pharmacy, or equivalent life sciences degree • A minimum of 2-3 years pharmaceutical industry experience working under GMP standards. • Preferably experience with stability studies (design, reporting, ICH requirements) • Understanding of analytical methods qualification and validation • Knowledge of data trending
Other informationThis is a fixed-term assignment for a maternity leave cover. There may be possibilities elsewhere in the company after this assignment finishes in case of strong performance, and this will be fully supported.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.