EMES Developer - Senior Principal Engineer
Bristol-Myers Squibb · Hyderabad · onsite · Posted 1d ago
About a minute. You'll make an account on the way through.
About this role
Job 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
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
About Bristol-Myers Squibb

Bristol-Myers Squibb
Pharma
375
employees
1887
139 years old
New York
United States
₹19.1L PA avg
Avg at Bristol-Myers Squibb
About
Industries
Employee ratings
10 reviews
Culture
2.6
Career growth
2.2
Work-life
3.1
Employees rate it well for
Find them on