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As a Regulatory CMC Associate, you will generate CMC documentation to support lifecycle submissions and keep business wide electronic systems up to date to maintain regulatory status up to the approval of CMC documentation supplied by Operations to Global Regulatory Affairs.
You will work with colleagues and other functions within AstraZeneca to obtain information that supports the generation of regulatory CMC documentation.
You may also support externalisation projects and the transfer of CMC documentation to external partners.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.
Nyckelord | Regulatory Documentation, Drug Development, Drug Discovery, product maintenance, Quality Control, Regulatory Affairs |
Branschkategori | Hälsa / Sjukvård |
Bransch | Apotekstjänster / läkemedel |
Arbetsgivare | Talentor Sweden AB |
Södertälje | |
Hemsida | www.astrazeneca.se/ |
Titel | Regulatory CMC Associate - AstraZeneca |
Sektor | Privat |
Tjänst | Heltid |
Anställningsform | Projekt |
Antal tjänster | 1 |
Ekaterina Leonova ekaterina.leonova@talentor.com +46(0)701976549 |