Bristol-Myers Squibb

EMES Developer

New Brunswick, New Jersey, United States

Not SpecifiedCompensation
Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceutical, ManufacturingIndustries

Requirements

Candidates should possess a Bachelor’s degree in Engineering, Computer Science, or a related field, with a minimum of 5 years of experience in the Life Sciences industry 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. They should have at least 5 years of direct experience designing, building, deploying, and supporting automation and execution systems (Syncade, DeltaV, PI Data historian, etc.) in regulated manufacturing environments, and demonstrate strong domain expertise in automation and execution systems.

Responsibilities

The EMES Developer will be responsible for development, maintenance, and support of the global Enterprise Manufacturing Execution Systems (EMES) solution, partnering with IT and Business teams to understand requirements and develop solutions. They will design, build, test, and deliver standard and custom EMES capabilities, provide support to minimize disruption to manufacturing, contribute to knowledge management, promote compliance with data integrity and computer system validation requirements, and identify opportunities for continuous improvement.

Skills

Emerson Syncade MES
Automation
Execution Systems
DeltaV
PI Data Historian
Data Integrity
Computer System Validation
Manufacturing
Requirements Gathering
Solution Design
Support
Maintenance
Development
Testing
Domain Expertise

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

Key Metrics

New York City, New YorkHeadquarters
1887Year Founded
$33,706.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Benefits

Flexible Work Hours
Hybrid Work Options
Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.
BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.
Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.
The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.
BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.
The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.
BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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