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Chemist scientist • petershausen

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Scientist (m / f / x) GMP manufacturing ADC

Scientist (m / f / x) GMP manufacturing ADC

Daiichi Sankyo Europe GmbHPfaffenhofen an der Ilm, Deutschland
With over 120 years of experience and approximately 19,000 employees in more than 30 countries / regions, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care ...Mehr anzeigenZuletzt aktualisiert: vor 3 Tagen
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Scientist (m / f / x) GMP manufacturing ADC

Scientist (m / f / x) GMP manufacturing ADC

Daiichi Sankyo Europe GmbHPfaffenhofen an der Ilm, Deutschland
Vor 3 Tagen
Stellenbeschreibung

With over 120 years of experience and approximately 19,000 employees in more than 30 countries / regions, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.

In Europe, we focus on two areas : The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life.

In Oncology, we are driving innovation in solid tumours and blood cancers, founded on breakthrough science from our own labs in Japan. We aspire to create better tomorrows for people living with cancer and their loved ones.

Our European headquarters are in Munich, Germany, and we have affiliates in 15 European countries and Canada.

For our development and production site in Pfaffenhofen an der Ilm or our Munich office we are seeking highly qualified candidates to fill the position :

Scientist (m / f / x) GMP manufacturing ADC

The position :

The Scientist GMP manufacturing ADC will be a key contributor to the establishment of a new drug substance production unit for Antibody-Drug Conjugates (ADC) at the site in Pfaffenhofen. Your primary role will be to support the establishment of the new production facility as expert from GMP perspective, including the generation of the required GMP documents. Once the facility is up and running, your task will be to contribute to all operations and maintenance in this GMP bioconjugation facility. You task will include to ensure performance of your tasks in compliance with the regulatory requirements and collaborating with other departments to support manufacturing with good quality.

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