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 engaging 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.
Job Description
Key Responsibilities
- This position is responsible for facilitating the initiation of commercial stability studies, tracking the enrollment of stability batches,
assembling, analyzing and reporting of stability data.
- The responsibilities include authoring stability initiation documents and other related documents including the Master Stability Protocols, Study Specific Protocols, CMO Stability protocols and Batch enrollment forms.
- Responsible for creation and tracking of the stability annual requirements, and year end requirement check
- Responsible for batch identification as per annual program
- Responsible for LIMS study creation and data management.
- Responsible for stability data entry, reporting and trending into reports (e.g. Annual Product Quality Reports, Annual Reports, Annual Product Stability Reviews, and other reports).
- Assembles, reviews and trends stability data from either internal or external sources using statistical packages (e.g. JMP).
- Develops and maintains expertise on the overall stability performance of products manufac