**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Senior Scientist **Location** : Summit, New Jersey **Business Unit Overview** Our Drug Product Development team is committed to CMC design, development, and commercialization of innovative drug products to improve patient lives. We leverage the best people, collaboration, and cutting-edge innovation to achieve this commitment. BMS's internal engine of innovation includes unrivaled industry leading expertise in CMC development of small molecules, protein biotherapeutics, protein degraders, and other therapeutic modalities. We collaborate closely with our colleagues in R&D and Commercial to design our drug products. Here, you'll get the chance to grow and thrive through opportunities that are uncommon in scale and scope. **Position Summary** As a Senior Scientist, the selected candidate will be responsible for development of analytical methods in support of solid oral and sterile drug product development and commercialization. The Senior Scientist will facilitate analytical problem solving in the development of drug product programs and participate as a member of a multidisciplinary drug product development team. This position requires significant collaborative interaction with drug product development scientists and scientists in GMP operations. The successful candidate will utilize various analytical techniques in problem solving and analysis of drug product formulations and must be able to effectively communicate with other team members and key stakeholders. The Senior Scientist may also serve as a drug product analytical lead who will drive analytical strategy and support for small molecule drug product development activities. **Key Responsibilities** The Senior Scientist will collaborate as an individual contributor or drug product analytical lead within project matrix teams for multiple development candidates across BMS sites to develop analytical methodology to support stability and release of clinical drug product and will also support drug product formulation and process development including characterization of the process and finished product. This includes: + Development of drug product analytical methods including chromatography-based methods such as HPLC/UPLC/SEC/GC, Dissolution, LC-MS, KF and electrophoretic-based methods such as iCIEF/CGE/CZE. + Critical analysis of analytical results with the goal of improving the robustness of analytical methods and enhancing understanding of key drug product quality attributes. + Conduct and assess developmental stability experiments to inform formulation design and packaging selection for drug products. + Review and discuss analytical results and conclusions both orally and in writing. **Qualifications & Experience** **Required:** + Completed BS and minimum of 7 years; MS and minimum of 4 years; or Ph.D. and minimum of 2 years in Chemistry (or relevant discipline) with pharmaceutical laboratory experience in the core analytical techniques of HPLC and Dissolution. + Extensive experience with various analytical techniques including HPLC, Dissolution and KF. + Ability to independently execute and document scientific experiments and effectively communicate study results. + Demonstrated problem solving skills and strong desire to grow scientifically. + The ability to collaborate and work effectively with individuals and as part of cross-functional teams. + Strong written and oral communication skills. **Ideal Candidates Would Also Have:** + Knowledge in analytical method development validation requirements as defined by ICH. + Familiarity with modern laboratory equipment and automation. + Understanding in formulation development, pharmaceutical processing related to drug product development. + Experience in building the CMC dossier for regulatory submissions within the development section as an author/reviewer. + Experience with Capillary Electrophoresis. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. **Company:** Bristol-Myers Squibb **Req Number:** R1585817 **Updated:** 2024-09-29 01:59:29.487 UTC **Location:** Summit West-NJ Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.