$92,160 - 138,240 yearly
Number of Applicants
:000+
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At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Education Qualifications
Musth have an Associate's Degree or higher required
Experience Qualifications
4 or more years of professional pharmaceutical industry experience managing GxP document management and training activities in the pharmaceutical or biotech industry, or equivalent experience is required.
Must have proven experience working with GXP principles required
Experience working in Veeva Quality Docs & ComplianceWire highly preferred.
Must have strong software and computer skills and MS Office applications (proficient in Teams, Excel)
Knowledge of UAT or Validation experience
Must have a proactive and positive approach to providing solutions
Ability to operate independently and to make informed decisions
Ability to work with cross-functional teams within a global matrixed environment.
Must have the ability to participate on early morning or late evening global calls.
Travel Requirements
Ability to travel up to 5% of the time domestic and international.
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.
Salary Range:
USD$92,160.00 - USD$138,240.00
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