Senior Automation Engineer (DeltaV) at Bristol-Myers Squibb

Devens, Massachusetts, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, BiotechnologyIndustries

Requirements

BS in Chemical Engineering/Electrical Engineering or any related equivalent engineering field
Minimum 9 years of industry experience on DeltaV distributed control systems
Minimum of 2 years of experience in Pharmaceutical or Biotechnology industries
In-depth understanding of ISA S88 and batch processing operations
Experience on Manufacturing Execution System (Syncade) preferable
Experience on OSI PI data historian applications preferable
Experience on automation validation (DeltaV, MES, PI) in GMP environment that includes test script generation and execution
Experience in executing Factory Acceptance Tests, supporting commissioning activities (hardware loop checks, cabinet testing)
Experience on change control management, deviation logs, and investigation under FDA regulated environment
Understanding of engineering documentation such as P&IDs, Process Flow diagrams and standard operating procedures
Strong interpersonal skills and ability to work in a team environment
Strong communication skills including oral and formal presentations
Ability to work in fast paced multi-tasking environment
Ability to troubleshoot control systems from field element up through operator interfaces and databases preferred
Ability to work with visual basics scripting preferred
Ability to work independently

Responsibilities

Support the operations on all GMP manufacturing systems (Process Automation System) in the Manufacturing Facilities in Devens, MA
Lead as well as participate in automation engineering initiatives in supporting manufacturing operations, system enhancements and site expansion activities for Clinical manufacturing and Biologics development operations, involving design, configuration, integration, test process control systems
Participate in cross functional teams (system integrators, contractors, end users) to develop the design requirement specifications, test plans and protocols, including design specifications, functional specification, FAT protocols, SAT protocols
Plan, implement and test design following good automation practices and standard operating procedure
Provide support to shift engineers in troubleshooting and guide in resolution for manufacturing activities
Troubleshoot control systems from field devices up to operator interfaces and databases
Work in collaboration with Validation, Quality and Manufacturing Engineering and Manufacturing operations to keep the operations on site functional

Skills

Key technologies and capabilities for this role

DeltaVGMPProcess AutomationControl SystemsFAT ProtocolsSAT ProtocolsTroubleshootingFunctional SpecificationsConfigurationIntegrationDesign Specifications

Questions & Answers

Common questions about this position

What is the location for this Senior Automation Engineer role?

The role is based in Manufacturing Facilities in Devens, MA.

What experience is required for this position?

Candidates need a BS in Chemical Engineering, Electrical Engineering, or related field, minimum 9 years of industry experience on DeltaV distributed control systems, and at least 2 years in Pharmaceutical or Biotechnology industries.

What is the salary range for this role?

This information is not specified in the job description.

What is the company culture like at Bristol Myers Squibb?

The culture is described as challenging, meaningful, and life-changing, with uniquely interesting work, opportunities to grow alongside high-achieving teams, and emphasis on balance and flexibility.

What skills make a strong candidate for this role?

Strong candidates will have in-depth understanding of ISA S88 and batch processing, experience with automation validation in GMP environments, Factory Acceptance Tests, commissioning activities, and change control management under FDA regulations.

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.

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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