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USP seeks a Scientist III to lead the synthesis of USP Reference Standard candidate materials and API impurities. The role involves planning synthetic strategies, literature searches, and executing multi-scale synthesis from milligram to kilogram levels.
You will ensure quality, safety, and timely project completion while adhering to QMS and lab policies. Candidate will collaborate with teams to deliver targeted materials, prepare technical reports, and communicate progress to stakeholders.
At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
The incumbent will be responsible for the synthesis and delivery of USP Reference Standard candidate materials and API impurities through the design and development of safe, efficient, and cost-effective synthetic routes. The role involves conducting comprehensive literature searches using scientific databases, planning synthetic strategies, and executing the synthesis of target molecules from milligram to multigram/kilogram scale. The candidate will be expected to ensure the timely completion of assigned projects, prepare technical reports, effectively communicate project progress to stakeholders, and collaborate closely with team members to achieve project objectives. In addition, the individual must adhere to Quality Management System (QMS) requirements and follow laboratory safety policies.
As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
The [Scientist III] has the following responsibilities:
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
(Or)
M Sc (Organic Chemistry) from a reputed university with minimum 6-8 years of industrial experience in API Process R&D/CDMO/CRO
Desired preferences include highlighting any additional preferred levels of expertise for the role—reminder: items listed here are not requirements and do not disqualify a candidate from consideration.
None, this is an individual contributor role.
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement