Posted in Science 11 days ago.
Type: Full-Time
Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us.
Hybrid
Employee Value Proposition:
Join our team at Taiho Oncology where innovation thrives, and excellence is celebrated. As a Senior Manager in Analytical Development, you'll play a pivotal role in driving scientific breakthroughs and shaping the future of our industry. At Taiho, we prioritize collaboration, creativity, and continuous learning, providing you with the resources and support you need to excel in your role. With competitive compensation, a supportive work culture, and opportunities for career growth and advancement, Taiho is more than just a workplace – it's a community of passionate professionals dedicated to making a difference. Join us and unlock your full potential as a leader in analytical development.
Position Summary:
The Sr. Manager, Analytical Development is responsible for all aspects of Analytical Development related to drug substance and drug product, serving as analytical lead for assigned projects with the CMC team. Liaises with CMOs to ensure methods are developed and qualified to meet regulatory requirements, interacts with QA/Regulatory/CMC to set specifications, and ensures batches are tested and released to meet project timelines and clinical needs.
Performance Objectives:
Education/Certification Requirements:
Knowledge, Skills, and Abilities:
The pay range for this position at commencement of employment is expected to be between $153,000 – $181,000 annually; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as PTO, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.
If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
#LI-Hybrid
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