Join a Legacy of Innovation 110 Years and Counting!
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. 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, as well as other research areas centered around rare diseases and immune disorders.
ROLE SUMMARY
This role is accountable for planning, conducting and managing internal and external GVP qualification, routine and for cause (directed) audits, primarily based in the US, reporting to the Head, Global Audits & Compliance. Ideal candidate will have a strong PV background combined with expert audit experience.
RESPONSIBILITIES
Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.
General Qualifications
Education Qualifications (from an accredited college or university)
Experience Qualifications
Preferred Qualifications
Travel
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
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