Bristol Myers Squibb
Principal Scientist, Oral Product Development
Bristol Myers Squibb, New Brunswick, New Jersey, us, 08933
Principal Scientist, Oral Product Development
Working with Us
Bristol Myers Squibb ofrece a balance of challenging, meaningful work and opportunities to grow within an innovative environment. The Drug Product Development team focuses on CMC design, development, and commercialization of drug products to improve patient lives. The organization collaborates across R&D and Commercial teams to design drug products and enable development across all stages. Position Summary Bristol Myers Squibb is seeking a Principal Scientist to join the Oral Product Development group within the Drug Product Development function. This group supports formulation and process development for candidates from preclinical stages to commercial process readiness. The incumbent will be responsible for formulation design, development, characterization, and technology transfer to enable development of small molecule drug products (DPs). The role includes acting as an individual contributor and as a formulation matrix team lead, providing guidance on drug product control strategies across all development stages. Key Responsibilities Collaborate with Drug Product, Analytical, API, Quality, and Regulatory functions to execute formulation/process development, formulate strategies, and support regulatory submissions and approvals. Design, develop, and characterize robust small molecule drug product formulations for clinical studies and commercialization. Lead drug product formulation and process development, evaluating strategies to enhance oral bioavailability, stability, and processability. Support preparation of CMC regulatory documents. Contribute to departmental initiatives and methodologies. Maintain safety, regulatory, and compliance standards related to pharmaceutical development. Prepare technical reports, batch records, SOPs, publications, and oral presentations as required. Collaborate with cross-functional teams to develop and optimize formulations and enable technology transfer to CMOs and other sites for manufacturing and scale-up. Develop, coach, and mentor others. Qualifications & Experience Educational background: BS with minimum 9 years, or MS with minimum 6 years, or PhD with minimum 4 years in Pharmaceutical Science, Chemical Engineering, or related discipline with pharmaceutical development experience. Experience in formulation development and pharmaceutical processing related to drug product development. Strong understanding of drug substance, excipients, unit operations (blending, milling, sieving, granulation, tableting, encapsulation, coating, spray drying), critical quality attributes, statistics, risk assessment, and cGMP principles. Experience building CMC dossiers for regulatory submissions as an author/reviewer; basic regulatory knowledge. Demonstrated problem-solving and troubleshooting skills; strong experimental design and execution capabilities. Ability to work independently and provide leadership, guidance, and training within the department. Strong verbal and written communication, interpersonal, and cross-functional collaboration skills. Ability to lead workgroups and cross-functional teams, contribute to strategy development and execution, and support cultural initiatives. Compensation Overview New Brunswick, NJ, US: $138,190 - $167,457 for full-time employment. Additional incentive cash and stock opportunities may be available based on eligibility. Final compensation is based on demonstrated experience. Benefits vary by location and role; details at careers.bms.com/life-at-bms. On-site / Work Model BMS has a location-based occupancy model. Site-essential roles require 100% onsite work; site-by-design roles may offer hybrid work with at least 50% onsite; field-based and remote-by-design roles require travel to sites, patients, or partners as an essential job function. Equal Employment Opportunity & Accessibility BMS is committed to an accessible recruitment process and reasonable accommodations. Inquiries may be directed to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility for our EEO statement.
#J-18808-Ljbffr
Working with Us
Bristol Myers Squibb ofrece a balance of challenging, meaningful work and opportunities to grow within an innovative environment. The Drug Product Development team focuses on CMC design, development, and commercialization of drug products to improve patient lives. The organization collaborates across R&D and Commercial teams to design drug products and enable development across all stages. Position Summary Bristol Myers Squibb is seeking a Principal Scientist to join the Oral Product Development group within the Drug Product Development function. This group supports formulation and process development for candidates from preclinical stages to commercial process readiness. The incumbent will be responsible for formulation design, development, characterization, and technology transfer to enable development of small molecule drug products (DPs). The role includes acting as an individual contributor and as a formulation matrix team lead, providing guidance on drug product control strategies across all development stages. Key Responsibilities Collaborate with Drug Product, Analytical, API, Quality, and Regulatory functions to execute formulation/process development, formulate strategies, and support regulatory submissions and approvals. Design, develop, and characterize robust small molecule drug product formulations for clinical studies and commercialization. Lead drug product formulation and process development, evaluating strategies to enhance oral bioavailability, stability, and processability. Support preparation of CMC regulatory documents. Contribute to departmental initiatives and methodologies. Maintain safety, regulatory, and compliance standards related to pharmaceutical development. Prepare technical reports, batch records, SOPs, publications, and oral presentations as required. Collaborate with cross-functional teams to develop and optimize formulations and enable technology transfer to CMOs and other sites for manufacturing and scale-up. Develop, coach, and mentor others. Qualifications & Experience Educational background: BS with minimum 9 years, or MS with minimum 6 years, or PhD with minimum 4 years in Pharmaceutical Science, Chemical Engineering, or related discipline with pharmaceutical development experience. Experience in formulation development and pharmaceutical processing related to drug product development. Strong understanding of drug substance, excipients, unit operations (blending, milling, sieving, granulation, tableting, encapsulation, coating, spray drying), critical quality attributes, statistics, risk assessment, and cGMP principles. Experience building CMC dossiers for regulatory submissions as an author/reviewer; basic regulatory knowledge. Demonstrated problem-solving and troubleshooting skills; strong experimental design and execution capabilities. Ability to work independently and provide leadership, guidance, and training within the department. Strong verbal and written communication, interpersonal, and cross-functional collaboration skills. Ability to lead workgroups and cross-functional teams, contribute to strategy development and execution, and support cultural initiatives. Compensation Overview New Brunswick, NJ, US: $138,190 - $167,457 for full-time employment. Additional incentive cash and stock opportunities may be available based on eligibility. Final compensation is based on demonstrated experience. Benefits vary by location and role; details at careers.bms.com/life-at-bms. On-site / Work Model BMS has a location-based occupancy model. Site-essential roles require 100% onsite work; site-by-design roles may offer hybrid work with at least 50% onsite; field-based and remote-by-design roles require travel to sites, patients, or partners as an essential job function. Equal Employment Opportunity & Accessibility BMS is committed to an accessible recruitment process and reasonable accommodations. Inquiries may be directed to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility for our EEO statement.
#J-18808-Ljbffr