Passion for Innovation. Compassion for Patients.
With over 120 years of experience and more than 17,000 employees in over 20 countries, 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 strive to become a global pharma innovator with competitive advantage, creating novel therapies for people with cancer.
Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries and Canada.
For Daiichi Sankyo Europe GmbH we are seeking highly qualified candidates to fill the position:
Senior Quality Manager CMO (m/f/x) – Drug Product Manufacturing
Purpose of the function:
Roles and responsibilities:
1. Manage quality oversight at CMOs You are responsible for quality related topics like change control, deviations and/or complaints related to DS products at CMOs Define together with the CMO effective CAPAs and track the timely implementation As DS QA you independently review, evaluate and approve documents like APQRs, PPQ reports or CPVs The QM CMO is the person responsible for preparing and negotiating QAAs with CMOs and ensures the CMOs work in accordance with DS QAAs You are involved in establishment of new manufacturing processes and site transfer activities and act as quality subject matter expert supporting PPQ and validation activities You support CMOs during Authority Inspections and perform audits on behalf of DS at different suppliers as needed In this role you identify quality risks at our CMOs and escalate issues in case it becomes necessary
2. Act as global information distributor In your new role you support global teams and SMEs to identify and define quality needs for CMOs You share quality related information from the CMOs to our global stakeholders within the global QA environment as well as in department overarching meetings
3. Participate in the further development of the corporate QM-System In global working teams you act as SME to improve the DS quality system and global SOP landscape Share knowledge and expertise within QA or to other functions to improvement CMO management at DS
In this role you will work globally in close cooperation with other departments like Supply Chain, CMC, regulatory functions and others to ensure consistent supply to markets with products which meet our high quality standards at any time.
Personal skills and professional experience:
4. University/FH/Master degree in natural or pharmaceutical sciences - preferred in Pharmacy, Biotechnology, Microbiology or a comparable program
5. At least five years of relevant work experience in the pharmaceutical industry including:
6. at least two years in Quality Assurance and/or Quality Management – preferable in Shop Floor QA activities or as QA Oversight for Manufacturing Activities for Sterile Manufacturing
7. at least two years in a GxP environment in a Fill&Finish manufacturing department for sterile solutions and/or lyophilisates
8. Excellent knowledge of international GMP/GDP regulations
9. Expertise in parenteral biological manufacturing particularly in the manufacture of sterile medicinal products or of biological active substances is desired