Principal Scientist, Product Champion

About this role

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. 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 Summary: The Product Champion provides technical leadership related to new or existing sterile drug product(s). The Product Champion is responsible for a product(s) at one or more sites. This position is accountable for key life cycle management product(s), providing specialized expertise necessary to complement site capabilities for critical investigations, process improvement projects, technical transfer projects, etc.  A product champion is responsible for leading a matrix Drug Product team, driving the drug product book of work, ensuring product robustness and process monitoring.

Key Responsibilities: • Lead Aseptic Drug Product matrix team for a sterile product(s). Represents Drug Product (DP) on technical matters at Technical Product Team (TPT) • Manages DP book of work (BOW) and risk register. • Provides assistance to sites to resolve significant quality events, and provides input for complex change controls. • Informed on Local Change Controls. Endorse Global Change Controls and Responsible for Global Change Control Impact Assessments • Accountable and responsible for lifecycle documents such as Time Out of Refrigeration (TOR) • Review and co-author sections of the CMC filings and Information Requests (IRs) • Review and co-author End-to-End Robustness and End-to-End Annual Product Quality Reviews. Accountable for robustness action plan. • Collaborate on/Drive technology transfer (TT) project definition and support chartered projects. • Support Technology Transfers, providing input, reviewing/approving key documents. Identifying issues, resolving roadblocks, and informing the team of similar scenarios/learnings from other projects/sites. • Interact and engage with a core team of specialized experts with necessary capabilities to support the BMS portfolio of products and complement site capabilities. • Drives DP Strategy and direction within DP sub-team, TPT meetings, etc. • Demonstrates leadership behaviors, engaging the right team members to enable decision making and successful project execution. • Can work independently with little direction. • Report into Product Champion Cluster Lead; may report into TT group or Lifecycle Team Lead as needed with dotted line into Product Champion (PC) team. • Up to 30% travel

Qualifications & Experience: Required: • Bachelor’s degree with 9+ years of relevant experience; Master's/Ph.D. preferred. Time spent in advanced degree program may consider as equivalent experience. • In-depth knowledge in Biologics/sterile liquid drug products, aseptic processing • Experience in Biologics/Vaccine Aseptic Drug Product Manufacturing and/or Technology Transfer • Ability to serve as a technical expert for a Drug Product manufacturing site • Strong critical thinking, technical writing, and verbal communication • Ability to work independently (or under limited supervision) • Demonstrated ability to work in a matrix environment and effectively support the decentralized manufacturing function. • Demonstrated ability to build alignment with business partners including analytical, regulatory, and manufacturing regional and site leaders. • Demonstrated ability to influence areas not under direct control to achieve objectives. • Demonstrated ability to make decisions that frequently require developing new options to solve complex problems.

Desired: • Experience in Lyophilization technology and ability to serve as technical expert for Lyophilization • Thorough knowledge of quality systems, Quality by Design, validation principles for product and engineering design and process control fundamentals • Working competency of Statistical Process Control and related tools is desired • Experience with regulatory filings and/or Health Authority questions.

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.

Compensation Overview:

New Brunswick - NJ - US: $123,580 - $149,752
 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. 

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.   Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: • Health Coverage: Medical, pharmacy, dental, and vision care.

• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).

• Financial Well-being and Protection: 401(k) plan, short- an

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