Head of Chromatography Laboratory
Vor 7 Tagen
About Daiichi Sankyo Europe
Daiichi Sankyo Europe is a leading pharmaceutical company dedicated to improving the quality of life for patients worldwide. With a presence in over 20 countries, we have a team of over 17,000 employees who are passionate about research, development, and production of innovative therapies.
Our Mission
We are committed to protecting people from cardiovascular diseases, the leading cause of death in Europe, and developing innovative treatments for cancer. Our European and German headquarters are located in Munich, and we have subsidiaries in 13 European countries and Canada, making us one of the largest Japanese pharmaceutical companies in Europe.
About the Role
We are seeking a highly skilled and experienced professional to join our Quality Control team in our production facility in Pfaffenhofen/Ilm. As the Head of Chromatography Laboratory, you will be responsible for leading our LC/GC (Liquid and Gas Chromatography) laboratory for the analytical testing of pharmaceutical products.
Key Responsibilities
- Lead the LC/GC laboratory team and ensure the effective operation of the laboratory, including the maintenance of equipment and the development of new analytical methods.
- Develop and implement quality control procedures to ensure the accuracy and reliability of analytical results.
- Collaborate with cross-functional teams to ensure the quality of raw materials, intermediates, and finished products.
- Develop and maintain analytical methods and procedures to ensure compliance with regulatory requirements.
- Provide technical expertise and support to the quality control team and other departments as needed.
- Ensure the laboratory is equipped with the necessary resources and equipment to perform its duties effectively.
- Develop and implement training programs for laboratory personnel to ensure they have the necessary skills and knowledge to perform their duties effectively.
- Ensure compliance with regulatory requirements and company policies and procedures.
Requirements
- PhD in a relevant field (Pharmaceutical Chemistry, Analytical Chemistry, Biochemistry, Biology, Biotechnology) or equivalent experience.
- Extensive experience in LC/GC/MS and Empower with a strong understanding of pharmaceutical analysis and quality management/GMP.
- Excellent communication and leadership skills.
- Ability to work independently and as part of a team.
- Strong problem-solving and analytical skills.
What We Offer
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and experienced professional looking for a new challenge, please submit your application.
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