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EMES Developer id-9299

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.

 

 

Summary:

Responsible for development, maintenance and support of the global Enterprise Manufacturing Execution Systems (EMES) solution that is utilized globally across the digital manufacturing network to produce medicine.

The EMES Developer's scope is EMES core platform, components, interfaces, custom tools, and any customizations that support digital manufacturing systems and operations including:

 

Specific Responsibilities:

  • Partner with IT and Business teams to understand requirements and develop solutions

  • Design, build, test and deliver standard and custom EMES capabilities to the global manufacturing network

  • Provide support of the EMES solution to minimize disruption to manufacturing and/or impact to product

  • Support administration of the central EMES development and test systems, with oversight over site EMES development, test, and production systems

  • Contribute to knowledge management strategy through content generation and mentoring

  • Identity and execute on opportunities for continuous improvement

  • 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 5+ years' Life Sciences industry experience and at least 5 years' experience in Emerson Syncade MES or 8+ years' experience in the Life Sciences industry, with at least 8 years' experience in Emerson Syncade MES

  • At least 5 years' direct experience designing, building, deploying and supporting 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 solution delivery

  • Ability to work across global sites and cultures.

  • Optional travel up to 5% 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.

 

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

 

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

 

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

 

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

 

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

 

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

 

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/

 

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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