Daiichi Sankyo Europe GmbH
81379 München - Deutschland
Pharmazeut/in
Arbeit
Vollzeit
ab 04.06.2026
Beschreibung
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, ...
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At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
For our Daiichi Sankyo Europe GmbH headquarters in Munich we are currently seeking highly qualified candidates to fill the position:
Expert (m/f/d) CMO Quality Management
As an Expert in CMO Quality Management, you will be a key player supporting the primary contact for quality-related topics at Contract Manufacturing Organizations (CMOs). Your role is essential in managing quality oversight at CMOs, ensuring the implementation and maintenance of Daiichi Sankyo's high-quality standards (GMP/GDP) and regulatory compliance for our oncology products. You will also collaborate across Daiichi Sankyo functions to support quality-related processes globally.
Lead quality oversight activities at CMOs to ensure compliance with Daiichi Sankyo standards and international GMP guidelines
Support and manage quality topics such as change control, deviations, and complaints related to Daiichi Sankyo products
Monitor and track timely implementation and effectiveness of CAPAs linked to deviations or audit findings in collaboration with CMOs and internal stakeholders
Review, evaluate, and approve critical quality documents including complaint investigations, deviation reports, and change controls, ensuring stakeholder involvement
Assist CMO Quality Managers during authority inspections at supplier sites
Collect and process quality data from CMOs according to internal SOPs, acting as a global information distributor
Collaborate with global teams and subject matter experts to identify and define quality needs for CMOs
Share quality-related information within global QA environments and cross-departmental meetings
Contribute to the ongoing development of the corporate Quality Management System (QMS) and support global working teams in improving quality systems and SOP landscapes
Work closely with departments such as Supply Chain, Technical Management, and Regulatory Affairs to ensure consistent supply of high-quality products to the market
Bachelor’s degree in natural or pharmaceutical sciences with a minimum of 3 years relevant experience OR vocational training in pharmaceutical business with at least 6 years relevant experience
Minimum 3 years professional experience in the pharmaceutical industry, including:
At least 1 year in Quality Assurance and/or Quality Management, preferably with shop floor QA or QA oversight in manufacturing
At least 2 years in a GxP environment in manufacturing or comparable roles
Strong knowledge of international GMP/GDP regulations
Assertive with excellent communication skills and a diplomatic approach during negotiations
Team player with high quality consciousness and a solution-oriented mindset
Fluent in English and German, both written and verbal
Experience managing CMOs or external suppliers is advantageous
Willingness to travel up to 10% domestically and internationally
Excellent Benefits
Work-Life Balance
Growth and Development
Health and Wellbeing Support
For our Daiichi Sankyo Europe GmbH headquarters in Munich we are currently seeking highly qualified candidates to fill the position:
Expert (m/f/d) CMO Quality Management
As an Expert in CMO Quality Management, you will be a key player supporting the primary contact for quality-related topics at Contract Manufacturing Organizations (CMOs). Your role is essential in managing quality oversight at CMOs, ensuring the implementation and maintenance of Daiichi Sankyo's high-quality standards (GMP/GDP) and regulatory compliance for our oncology products. You will also collaborate across Daiichi Sankyo functions to support quality-related processes globally.
Lead quality oversight activities at CMOs to ensure compliance with Daiichi Sankyo standards and international GMP guidelines
Support and manage quality topics such as change control, deviations, and complaints related to Daiichi Sankyo products
Monitor and track timely implementation and effectiveness of CAPAs linked to deviations or audit findings in collaboration with CMOs and internal stakeholders
Review, evaluate, and approve critical quality documents including complaint investigations, deviation reports, and change controls, ensuring stakeholder involvement
Assist CMO Quality Managers during authority inspections at supplier sites
Collect and process quality data from CMOs according to internal SOPs, acting as a global information distributor
Collaborate with global teams and subject matter experts to identify and define quality needs for CMOs
Share quality-related information within global QA environments and cross-departmental meetings
Contribute to the ongoing development of the corporate Quality Management System (QMS) and support global working teams in improving quality systems and SOP landscapes
Work closely with departments such as Supply Chain, Technical Management, and Regulatory Affairs to ensure consistent supply of high-quality products to the market
Bachelor’s degree in natural or pharmaceutical sciences with a minimum of 3 years relevant experience OR vocational training in pharmaceutical business with at least 6 years relevant experience
Minimum 3 years professional experience in the pharmaceutical industry, including:
At least 1 year in Quality Assurance and/or Quality Management, preferably with shop floor QA or QA oversight in manufacturing
At least 2 years in a GxP environment in manufacturing or comparable roles
Strong knowledge of international GMP/GDP regulations
Assertive with excellent communication skills and a diplomatic approach during negotiations
Team player with high quality consciousness and a solution-oriented mindset
Fluent in English and German, both written and verbal
Experience managing CMOs or external suppliers is advantageous
Willingness to travel up to 10% domestically and internationally
Excellent Benefits
Work-Life Balance
Growth and Development
Health and Wellbeing Support
Ref-Nr.: 11091052
Aktualisiert:
06.06.2026
Quelle: Bundesagentur für Arbeit
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Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
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