Daiichi Sankyo and its 15.000 employees in more than 20 countries are dedicated to the creation and supply of innovative pharmaceutical products. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology. Our European headquarters are in Munich, Germany and we have affiliates in 13 European countries including Denmark, where Copenhagen acts as the Nordic headquarter.
For our headquarter in Munich we are seeking highly qualified candidates to fill the position:
Quality Control Manager (m/f/x) for Pharmacovigilance
Purpose of the function:
The Quality Control Manager will work with Quality & Compliance Lead to maintain and enhance Daiichi Sankyo PV Quality Management System in collaboration with other regional teams in the US and Japan and maintains Pharmacovigilance System Master File (PSMF). This position is responsible for the quality control of PV tasks fulfilled by DSE (EU headquarter office), EU affiliates, CROs and license partners and proactively monitors quality of all PV tasks (including compliance monitoring) and ensures operational standards are well-maintained.
This position is also expected to contribute to the global projects together with Quality & Compliance Lead to enhance Daiichi Sankyo Global PV Quality Management System by implementing further globally harmonized standards and validated tools for process improvement, automation and trend analysis.
We offer an interesting, diversified and challenging position, good contractual conditions, flexible working models, all the social benefits of a modern company and a professional environment where you will have the opportunity for personal growth.