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 .
Key Responsibilities:
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- Support global recipe management strategy to maximize reuse of recipes and/or recipe segments across sites
- Build recipes that are designed around simplicity, flexibility, and cost effectiveness
- Update recipes deployed at operational sites and participate in harmonizing recipes across all Cell Therapy sites
- Partner with MS&T and Process Robustness team to configure recipes in support of analytics
- Partnering with Supply Chain, MS&T, Quality, and Manufacturing Operations to understand business requirements
- Development of functional specifications
- Recipe authoring, demos , and dry run facilitation
- Recipe User Acceptance Testing
- Recipe and master data installations and promotions
- Ensure recipes are built with consistency and adhere to guidelines
- Perform recipe and specification review and approvals
- Gather and m anage requirements around batch reports that relate to the Review by Exception and Release by Exception strategies
- Tier 3 escalation support of Cell Therapy recipes and process to minimize disruption to manufacturing and/or impact to product
- Support strategy for collecting end user feedback and improving the usability and user experience of the overall EMES solution
- Support risk and impact assessment that changes, patches, outages or other events can have to the E MES solution and the global network and define mitigation strategies.
- Support a knowledge management strategy including generating training content and mentoring
- Promote compliance with data integrity and computer system validation requirements and regulations
- Promote compliance by understanding change and the impact to the validated state of the application and underlying infrastructure.Qualifications
- Bachelor of Science in Engineering, Computer Science or related fields with 2 + years’ Life Sciences industry experience and preferably 1 years’ experience in Emerson Syncade MES
- E xperience in designing and building recipes in automation and execution systems ( Syncade , DeltaV , PI Data historian, etc.) in regulated manufacturing environments
- Strong domain expertise in the application of IT to manufacturing, including a broad understanding of processes and how they are supported by IT tools and systems.
- Strong knowledge of regulatory landscape and demonstrated experience with software validation.
- Proven track record of successful IT/automation project delivery
- Ability to work across global sites and cultures.
- Ability to travel up to 10 % domestically and internationally
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.

Please refer the Job description for details