Subskrypcja powiadomień powiodła się. Będziesz jednym z pierwszych, którzy dowiedzą się o podobnych zleceniach. Zawsze możesz zmienić wyrażone uprawnienia w ustawieniach przeglądarki.
The Company Our client is a global leader in healthcare and pharmaceutical products, with base in Leiden. Their mission is to transform individual lives and fundamentally change the way diseases are interpreted, managed and in the end prevented. In over 150 countries the company is bringing innovative science and together with the most creative minds in the industry.
Role Description As an Associate Analyst you will coordinate the release of raw materials drug substance and drug products from internal and external stakeholders. Ensuring on-time delivery of results per agreed timelines.
Responsibilities
- Coordinate the stability testing of large molecule products according to local procedures and agreed timelines - Acting as a subject matter expert on release and stability processes with a leading role during GMP inspections - Participation in meetings of the quality network organization and partner with customers - Responsible to coordinate all data requests provided by various stakeholders - Lead and drive continuous improvement projects - Adhere to compliance best practices, EHSS regulations and lean principles
Requirements
- Bachelor's Degree in a relevant discipline with 2-4 years' of related working experience - Advanced knowledge on lab systems and lab environment, data integrity and data management - Knowledge of statistical data analyses - Lean/BE experience - Proactive stakeholder management
Other Information As Associate Analyst you are acquainted with the annual company and division goals and you are aware of how you can influence these through your performance.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Czy chcesz otrzymywać oferty pracy na podobne stanowiska?
