Job description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. 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: · Material and Inventory modules · Order management · Equipment and instrument integration · Sample management · Patient scheduling system integration · Label printing · General automatic recipe functionality · Custom business recipe capabilities · Batch reporting and analytics 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 (preferred) or related fields • 10+ years’ experience in the Life Sciences industry, with at least 8 years’ experience in 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 • Proficiency in scripting and automation using VBScript, PowerShell, Python, or JavaScript. • Strong skills in SQL Server, including query optimization, complex querying, and database administration. • Knowledge of message-oriented middleware and event-driven systems, including MSMQ, Kafka, RabbitMQ, or similar technologies. • Experience in Enterprise System Integration, preferably involving SAP, LIMS, and MES platforms • Ability to work across global sites and cultures. • Optional travel up to 5% domestically and internationally We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. Compensation Overview: Devens - MA - US: $174,750 - $211,758 Madison - Giralda - NJ - US: $158,870 - $192,507 New Brunswick - NJ - US: $158,870 - $192,507 Princeton - NJ - US: $158,870 - $192,507 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance. Benefits: Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at careers.bms.com How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at careers.bms.com. Supporting People with Disabilities 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. Candidate Rights BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: 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: careers.bms.com Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at careers.bms.com . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account. R1607674 : EMES Developer - Senior Principal Engineer

Requirements

Must-haves

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:
Material and Inventory modules
Order management
Equipment and instrument integration
Sample management
Patient scheduling system integration
Label printing
General automatic recipe functionality
Custom business recipe capabilities
Batch reporting and analytics
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.
10+ years’ experience in the Life Sciences industry, with at least 8 years’ experience in 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.

Nice-to-haves

Bachelor of Science in Engineering, Computer Science (preferred) or related fields

Application prep

Use the role’s language and application details while tailoring your materials.

Keywords to mirror

pythonjavascriptsqlaccessibility

Platform: eightfold
Effort: medium

Benefits

Benefits detected in the listing.

Dental

Vision

Paid Time Off