Coordinator Product Stability
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 organisation, based in Zuid-Holland Netherlands.
The CompanyTheir product stability team is part of the Analytical Development Department 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.
Role DescriptionThe Coordinator will be a key player in the support 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 various documents such as stability protocols, stability reports, amendments, shelf-life extensions.
ResponsibilitiesWe 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. 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.
RequirementsSince 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.
• 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, but no guarantees. Minimum Bachelor's degree education but also open to Master's and even PhD.
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.