Sr Scientist - Radiopharmaceutical Development & CMC jobs in United States
cer-icon
Apply on Employer Site
company-logo

Bristol Myers Squibb · 2 months ago

Sr Scientist - Radiopharmaceutical Development & CMC

Bristol Myers Squibb is a dynamic biotechnology company focused on improving survival of people with cancer. They are seeking a highly motivated Sr. Scientist to lead the development and optimization of radiopharmaceutical drug products and radioisotopes, playing a pivotal role in preclinical development aimed at treating various cancers.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
check
H1B Sponsor Likelynote

Responsibilities

Design, plan and execute scientific experiments for pre-clinical development of radiopharmaceuticals
Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition, ensuring scalability and compliance with regulatory standards
Design, plan and execute scientific experiments for scale up and automation of drug products and API manufacturing processes
Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings in technical reports, regulatory documentation, and presentations for internal and external stakeholders
Author technical reports and source documents to support regulatory filing
Author CMC sections for IND/NDA for FDA submissions, and support regulatory filing in other jurisdictions, e.g. EMA, Health Canada, etc
Support technology transfer of drug products and API from preclinical stage to clinical manufacturing
Collaborate cross-functionally with Regulatory, Quality, Supply Chain, Clinical, and R&D teams to ensure alignment with corporate goals
Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates
Provide support for commercialization of radiopharmaceuticals
Up to 20% of travel required

Qualification

GMP regulationsFDA/EMA regulationsDrug developmentTechnical writingProject managementCross-functional collaborationProblem-solving

Required

Ph.D., M.S., or B.S. in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field, with requisite industry experience
5+ years of experience in drug development, manufacturing, CMC or related fields in a pharmaceutical industry, preferably radiopharmaceuticals
Strong understanding of GMP, FDA/EMA regulations, and ICH guidelines
Strong problem-solving abilities and the ability to manage multiple projects in a fast-paced environment
Excellent project management and cross-functional collaboration skills
Excellent technical writing skills

Benefits

Medical, pharmacy, dental and vision care
Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
Financial well-being resources and a 401(K)
Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support
Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility
Parental, caregiver, bereavement, and military leave
Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources
Tuition reimbursement
Recognition program

Company

Bristol Myers Squibb

company-logo
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.

H1B Sponsorship

Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)

Funding

Current Stage
Public Company
Total Funding
$29.32B
Key Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B

Leadership Team

leader-logo
Charles Bancroft
CFO
linkedin
leader-logo
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
linkedin
Company data provided by crunchbase