2 Chemical Processesreactions Jobs

At USP, inclusive scientific collaboration is highly valued, recognizing the importance of diverse expertise in strengthening the development of trusted public health standards. The organizational culture at USP supports equitable access to mentorship, professional development, and leadership opportunities, reflecting the belief that broad participation in scientific leadership leads to more impactful global health outcomes. As an equal employment opportunity employer, USP is committed to fair, merit-based selection processes that enable the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Reasonable accommodations are provided to individuals with disabilities, and policies are in place to create an inclusive and collaborative work environment. This non-supervisory position at USP involves supporting the process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. The successful applicant will work on projects, including Analytical Method Development and evaluation for in-process samples in synthetic chemistry. Responsibilities also include performing a variety of routine and non-routine analytical tests, maintaining safety and GLP environment in the lab, development/validation of methods, stability studies, and research projects in analytical chemistry. The role requires directing, troubleshooting, and sharing insights on complex projects, collaborating closely with other scientists and/or USP personnel. As part of the mission to advance scientific rigor and public health standards, the individual in this position will contribute significantly to increasing global access to high-quality medicines through public standards and related programs. USP emphasizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure that health systems worldwide can rely on strong, tested, and globally relevant quality standards. The People and Culture division at USP, in collaboration with the Equity Office, invests in leadership and workforce development to equip all employees with the skills necessary 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 IV at USP will have responsibilities including supporting reaction monitoring, scale-up, and final analysis of samples, preparing development reports, executing projects as per specifications, timelines, and budget, reviewing SOPs, protocols, reports, and more. Collaboration with the synthetics team, evaluation and implementation of Process Analytical Technologies (PAT) capabilities, planning and completion of projects, participation in ISO-9001 certification, maintenance of GLP, and safety procedures in the lab are key aspects of the role. The successful candidate will have a Master's degree in Analytical Chemistry/Organic Chemistry/M. Pharm with 8-10 years of experience or a Ph.D. with 4-7 years of experience in Analytical Research and Development. Hands-on experience with chemical methods and various instruments, understanding of process analytical technology, analytical testing and development, technical writing, communication skills, and the ability to function in a team-oriented environment are essential qualifications. USP welcomes applications from individuals holding historically marginalized and/or underrepresented identities. Desired preferences include hands-on experience with PAT instruments and techniques, knowledge of API manufacturing and product testing, expertise with USP compendial methods and requirements, pharmaceutical laboratory experience, strong project management skills, and proficiency in data evaluation and problem-solving. USP provides benefits to protect the personal and financial well-being of employees and their families. USP, the U.S. Pharmacopeial Convention, is an independent scientific organization collaborating with top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. With a core value of Passion for Quality, USP aims to strengthen the supply of safe, quality medicines and supplements worldwide. In building an inclusive organizational culture, USP affirms the value of Diversity, Equity, Inclusion, and Belonging to ensure confidence in health and healthcare quality for all.,

At USP, we highly value inclusive scientific collaboration and acknowledge that attracting diverse expertise strengthens our ability to develop trusted public health standards. We cultivate an organizational culture that supports fair access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research embody our belief that ensuring broad participation in scientific leadership leads to stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is dedicated 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 offer reasonable accommodations to individuals with disabilities and uphold policies that foster an inclusive and collaborative work environment. This non-supervisory position is designed to support the process development and scale-up of Active Pharmaceutical Ingredient (API) and related materials. As a successful applicant in this role, you will work on projects involving Analytical Method Development and evaluation for in-process samples in synthetic chemistry. You will be responsible for performing a variety of non-routine and routine analytical tests, maintaining a safe & GLP environment in the lab, including the development/validation of methods, stability studies, and research projects in analytical chemistry. Additionally, you will direct, troubleshoot, and share insights on complex projects, draw independent conclusions about the results, and determine the project's next steps. Collaboration with other scientists and/or USP personnel will be a key aspect of this role. As part of USP's 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. Our organization prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure that health systems worldwide can rely on robust, tested, and globally relevant quality standards. The Scientist IV will have the following responsibilities: - Support reaction monitoring, scale-up, and final analysis of samples as per monograph / in-house procedures. - Prepare development reports for Synthetic Support projects. - Execute projects per approved test protocols. - Evaluate, implement, and enhance Process Analytical Technologies (PAT) capabilities in collaboration with the synthetics team. - Plan, execute, and complete projects as per specifications, timelines, and budget. - Prepare and review SOPs, protocols, reports, etc. - Coordinate with external vendors and relevant internal departments to ensure project requirements are met. - Ensure maintenance and calibration of equipment, IQ/OQ/PQ of new instruments, and preparation for ISO-9001 certification/recertification. - Maintain GLP and implement safety procedures in the lab. - Work on any other assigned tasks/lab management activities. - Collaborate within the team and cross-functional teams. - Learn and practice Diversity, Equity, Inclusion & Belonging culture. The successful candidate should have a demonstrated understanding of the organization's mission, a commitment to excellence through inclusive and equitable behaviors, and the ability to quickly build credibility with stakeholders. Additionally, the following competencies and experience are required: - MSc. in Analytical Chemistry / Organic Chemistry/M. Pharm with 8-10 years of experience or Ph.D. with 4-7 years of experience in Analytical Research and Development. - Hands-on experience with chemical methods and instruments like HPLC, GC, LC-MS, GC-MS, FTIR, UV-Visible, wet chemistry, etc. - Understanding of process analytical technology, chemometrics, and knowledge of in-line, online, at-line process analytical tools. - Experience in analytical testing and development with a focus on process analytical chemistry. - Comprehensive understanding of synthetic organic molecules development and analytical chemistry. - Ability to perform analytical method developments and validations. - Excellent technical writing and verbal communication skills. - Good interpersonal skills and ability to function in a team-oriented environment. USP welcomes applications from individuals with historically marginalized and/or underrepresented identities. Candidates possessing many, though perhaps not all, qualifications are encouraged to apply. Additional desired preferences include hands-on experience with PAT instruments, familiarity with a variety of software and laboratory information systems, knowledge of API manufacturing and product testing, expertise with USP compendial methods and requirements, and strong project management skills. USP provides benefits to protect the well-being of employees and their families, including company-paid time off, comprehensive healthcare options, and retirement savings. Please note that USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under a specific written agreement with USP.,