Job Description
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.
We are seeking a highly qualified candidate to fill the position in Pfaffenhofen or Munich:
Regional Staff Member (m/f/x) - Regional GMP/GDP QA
The Position:
Daiichi Sankyo is seeking a dedicated and skilled professional to join our Quality Management department at our Pfaffenhofen/Ilm or Munich location as a Regional Staff Member – GMP/GDP QA. This position is available immediately.
- Collect data and prepare progress reports, KPIs, and metrics for regional and global reporting, including monthly reports, management reviews, and quarterly quality reports.
- Support ad hoc global quality reporting by gathering data and providing contextual insights to regional QA Senior Management.
- Organize, moderate, and support regional meetings related to GMP/GDP QA.
- Serve as the primary regional contact for Global Instruction Review concerning GMP/GDP QA.
- Act as Project Management Officer (PMO) upon request for regional and global GMP/GDP QA projects.
- Assist the Head of Regional GMP/GDP QA SPS & MAH QA in strategic initiatives and objectives.
- Completed degree in natural sciences, pharmaceutical sciences, or a comparable qualification.
- Minimum of 3 years relevant professional experience within a GMP/GDP-regulated environment.
- Proven experience in project management.
- Experience in a pharmaceutical manufacturing environment is advantageous.
- Excellent communication skills with a strong background in stakeholder management.
- Strong analytical abilities and meticulous attention to detail, capable of conveying complex issues and concepts to diverse stakeholders.
- Fluency in both German and English, spoken and written.
- Excellent Benefits
- Work-Life Benefits
- Growth and Development
- Health and Wellbeing Support