Sr. Specialist
2 weeks ago
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 120 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. 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, as well as other research areas centered around rare diseases and immune disorders.
Summary
This position is responsible to support the implementation of the Global R&D PV QA organizational strategy. This position will proactively collaborate with other Global quality colleagues to drive the global QA vision and act as the US QA point person for Strategy & Operations. This position will support continuous process improvement initiatives, support the annual Global Quality Strategy Plan for R&D PV QA and track business objectives through partnership with the QA leadership team . Position is responsible for support at the global organizational level. This position has considerable latitude to make decisions without supervisor approval and solves problems while carrying out assigned tasks. Additionally, this position is responsible for upholding a strong commitment to confidentiality and routinely handles sensitive documents that may impact multiple organizational units or project teams. This position has advanced skills in technology systems, content creation, word processing software and data management software, and business emailing software as well as intermediate skills in database and research tools.
Responsibilities
Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.
Education Qualifications (from an accredited college or university)
A High School Diploma is required.Associate's Degree strongly preferredExperience Qualifications
4+ years of professional experience within the pharmaceutical industry working within Quality Assurance is required.Must have a broad understanding of Health Authority expectations in the areas of Pharmaceutical Development; working in a GxP regulated environment, pharmaceutical industry.Proven experience in training and curricula development experience, including oversight and administration of validated electronic systems such as Sharepoint, LMS, Trackwise Digital and other quality management systems.Strong interpersonal, communication, technical writing, negotiation and problem-solving skills with demonstrated ability to build collaborative relationshipsStrong project management skillsOrganizational awareness (e.g. inter-relationships of departments, business priorities), including experience working cross-functionally and in global teams.Candidate must be creative and show initiatives, be customer focused, results driven and be able to work effectively in a global environment.In depth knowledge and working experience with common computer software programs, i.e. MS Office Suite (Word, Excel, Access, Outlook, PowerPoint, Visio, MS Project)Physical Requirements: Shipping out large packages/boxes. Moving/arranging file folders in large quantities.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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