Associate Scientist Product Stability | Bsc/Msc | Zuid-Holland
SIRE Life Sciences®
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SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Zuid-Holland Netherlands.
The CompanyThey develop vaccines that are the first or best in their class and protect against some of the world's most life-threatening infectious diseases. The pathogens against which vaccines are developed include Ebola, Respiratory Syncytial Virus (RSV), Human Immunodeficiency Virus (HIV), Extra-intestinal Pathogenic E. coli (ExPEC), Methicillin-Resistant Staphylococcus Aureus (MRSA), polio and influenza.
Role DescriptionProduct stability team is part of the Analytical Development Department of and 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.
ResponsibilitiesThe Associate Scientist will be a key player supporting the stability team members in the daily management of stability studies of the novel vaccines during the clinical development. You will work in a multidisciplinary environment and focus on assisting the scientists in the team in the preparation of various documents such as stability protocols, stability reports, amendments, shelf-life extensions. You provide support to other stability scientists in the management of quality and compliance aspects, and you are responsible for the routine preparation of data tables and visual overviews, graphical representation of the stability data and statistical analyses.
Since different CMC projects are carried out by different members of the stability team, 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 and future growth.
Requirements• BS or MS degree in Biochemistry, Pharmacy, or equivalent life sciences degree
• Must have some years pharmaceutical industry experience.
• Must be organized, structured with great eye for details
• Must have affinity with statistical tools and data trending
• Preferably experience with working in the GMP environment
• Preferably exposure to Stability field
• Preferably prior lab-based exposure (for deeper understanding of the data they work with)
Other informationYou can submit your application before the 11th of November.
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.