Senior Manager, Digital Manufacturing, MES Business Capabilities

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.

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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 Business Capabilities lead scope is EMES Veeva, GPS, sampling, label printing, and custom business functionality including recipe and workflow capabilities, interfaces, and any customizations that support digital manufacturing systems and operations.

Specific Responsibilities:

• Partner with MS&T, Manufacturing Operations and QC/LIMS system teams to understand requirements and opportunities around EMES and LIMS integration to enable a seamless user experience

• Partner with Data Privacy Office and cybersecurity teams to improve the architecture and security of the EMES and Global Patient Scheduling (GPS) integration to protect sensitive information

• Partner with Veeva Vault team to improve the architecture and reliability of the EMES and Veeva integration to ensure a seamless user experience

• Define, manage, and deliver the EMES sampling and business capabilities roadmap to support changing/emerging technologies and the continuing maturity of digital manufacturing

• Design and manage a EMES to LIMS, Veeva, and GPS integration strategy that ensures seamless operation of EMES during an outage

• Partner with Sample Manager and Labware integration teams to manage and deliver updates to the EMES-LIMS interfaces

• Partner with Veeva Vault integration teams to manage and deliver updates to the EMES-Veeva interfaces

• Partner with GPS integration teams to manage and deliver updates to the EMES-GPS interfaces

• Manage and deliver enhancement and defect updates per business priority to the library of recipe objects and workflows that enable:

  • EMES and LIMS integration and management

  • EMES and GPS integration

  • Enable label printing capabilities

  • General automatic recipe functionality

  • Custom business recipe operations

• Design and manage a sampling master data management strategy that:

  • Maximizes productivity of business users who maintain data

  • Minimizes and/or eliminates data duplication between systems

  • Maximizes mistake proofing

• Assess the risk and impact that changes, patches, outages or other events can have to the EMES solution and the global network and define mitigation strategies.

• Solution owner and delivery lead for the EMES-LIMS, EMES-Veeva, EMES-GPS, label printing and custom business capabilities

• Partner with and support other EMES delivery leads in managing the global EMES solution and roadmap

• Tier 3 escalation support of the EMES solution to minimize disruption to manufacturing and/or impact to product

• Manage a technical resource team to deliver on-time and on-budget projects

• 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 10+ years experience with MES , preferably Emerson Syncade MES

• At least 10 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 project delivery

• Ability to work across global sites and cultures.

• Ability to travel up to 20% domestically and internationally

The starting compensation for this job is a range from $121,000 to $172,000, plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. 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 our BMS Career Site. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program

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 an inclusive culture, promoting diversity 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
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

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.

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