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Scientist, Clinical Supply Operations, OSD Manufacturing

Bristol Myers Squibb
New Brunswick, United Statesfull_timeVerifiedPosted 25 Jun 2024

About the 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 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.

Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow. As a member of our team, you will get the chance to play a pivotal role to positively impact patients’ lives while developing professionally to achieve your own career goals.

Role & Responsibilities:

The candidate will be responsible for the following operationally based activities:

  • Effectively oversee batch execution and supervise technicians to ensure product is made in accordance with pertinent specifications and cGMP requirements.
  • Adherence to group master manufacturing schedule and escalation to management when timelines are at risk.
  • Generation and review of GMP documentation as necessary, including, batch records, SOPs, Work Instructions, planned deviations, operation alerts, and CAPAs.
  • Coordinate activities with other departments to ensure timely release of products.
  • Interface with Pharmaceutics R&D to ensure proper technical transfer and scale-up of formulae and processes into Clinical Manufacturing and out to commercial manufacturing.
  • Complete batch feedback reports and provide recommendation for process, procedure, and batch record improvements to management.
  • The candidate will work on a variety of processes, including the use of state of the art containment and PAT technology.  
  • They will supervise in a complex and dynamic organization, working in concert with other members of Clinical Supply Manufacturing to coordinate equipment and manpower requirements. 
  • Participate in the development of procedures and guidelines leading to a clear vision, with short- and long-term goals, for clinical manufacturing planning and management, in alignment of the business goals of Clinical Supply Operations. 
  • Additionally, this position will participate in high performing teams which develop strategies for incorporating new technology, improving regulatory compliance, and improving technology transfer within the Bristol-Myers Squibb research and development organization.

Qualifications & Experience:

  • A B.E./B.S. in Engineering or in a related science field and 5+ years of experience, M.S. degree and 2-4 years of experience, or PhD and 0-2 years of experience
  • 3+ years' experience in pharmaceutical manufacturing and/or formulation required. 
  • Experience with solid dosage dose manufacturing, cGMPs, and product or process development is preferred. 
  • The ability to work in a GMP environment and the capability to plan and execute projects is required. 
  • The successful candidate will have the ability to lead and motivate others, the capability to solve process related problems and the command of effective communication skills.

Why You Should Apply

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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

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Company

Bristol Myers Squibb

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