Senior Automation Engineer (DeltaV)
Bristol-Myers Squibb
Senior Automation Engineer (DeltaV)
Job Description
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. The activities will involve 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. This includes 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. 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. 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 required. Experience on Manufacturing Execution System (Syncade) preferable. Experience on OSI PI data historian applications is 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) required. Experience on change control management, deviation logs, and investigation under FDA regulated environment is required. 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 is preferred. Ability to work with visual basics scripting is preferred. Ability to work independently.
Key Responsibilities
- Support operations on all GMP manufacturing systems in the Manufacturing Facilities in Devens, MA
- Lead and participate in automation engineering initiatives for manufacturing operations, system enhancements, and site expansion activities for Clinical manufacturing and Biologics development operations
- Design, configure, integrate, and test process control systems
- Participate in cross-functional teams to develop 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 procedures
- 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
- Collaborate with Validation, Quality, Manufacturing Engineering, and Manufacturing operations to keep site operations functional
Required Qualifications
- BS in Chemical Engineering, Electrical Engineering, or 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 in executing Factory Acceptance Tests and 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
Preferred Qualifications
- Experience on Manufacturing Execution System (Syncade)
- Experience on OSI PI data historian applications
- Experience on automation validation (DeltaV, MES, PI) in GMP environment including test script generation and execution
- Ability to troubleshoot control systems from field element up through operator interfaces and databases
- Ability to work with visual basics scripting
Skills Required
- Strong interpersonal skills and ability to work in a team environment
- Strong communication skills including oral and formal presentations
- Ability to work in a fast-paced multi-tasking environment
- Ability to work independently
Benefits & Perks
- 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
- Summer hours flexibility
Locations
- Devens MA, United States
Salary
Estimated Salary Rangemedium confidence
120,000 - 180,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Strong interpersonal skills and ability to work in a team environmentintermediate
- Strong communication skills including oral and formal presentationsintermediate
- Ability to work in a fast-paced multi-tasking environmentintermediate
- Ability to work independentlyintermediate
Required Qualifications
- BS in Chemical Engineering, Electrical Engineering, or related equivalent engineering field (experience)
- Minimum 9 years of industry experience on DeltaV distributed control systems (experience)
- Minimum of 2 years of experience in Pharmaceutical or Biotechnology industries (experience)
- In-depth understanding of ISA S88 and batch processing operations (experience)
- Experience in executing Factory Acceptance Tests and supporting commissioning activities (hardware loop checks, cabinet testing) (experience)
- Experience on change control management, deviation logs, and investigation under FDA regulated environment (experience)
- Understanding of engineering documentation such as P&IDs, Process Flow diagrams, and standard operating procedures (experience)
Preferred Qualifications
- Experience on Manufacturing Execution System (Syncade) (experience)
- Experience on OSI PI data historian applications (experience)
- Experience on automation validation (DeltaV, MES, PI) in GMP environment including test script generation and execution (experience)
- Ability to troubleshoot control systems from field element up through operator interfaces and databases (experience)
- Ability to work with visual basics scripting (experience)
Responsibilities
- Support operations on all GMP manufacturing systems in the Manufacturing Facilities in Devens, MA
- Lead and participate in automation engineering initiatives for manufacturing operations, system enhancements, and site expansion activities for Clinical manufacturing and Biologics development operations
- Design, configure, integrate, and test process control systems
- Participate in cross-functional teams to develop 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 procedures
- 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
- Collaborate with Validation, Quality, Manufacturing Engineering, and Manufacturing operations to keep site operations functional
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
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Answer 10 quick questions to check your fit for Senior Automation Engineer (DeltaV) @ Bristol-Myers Squibb.
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Senior Automation Engineer (DeltaV)
Bristol-Myers Squibb
Senior Automation Engineer (DeltaV)
Job Description
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. The activities will involve 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. This includes 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. 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. 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 required. Experience on Manufacturing Execution System (Syncade) preferable. Experience on OSI PI data historian applications is 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) required. Experience on change control management, deviation logs, and investigation under FDA regulated environment is required. 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 is preferred. Ability to work with visual basics scripting is preferred. Ability to work independently.
Key Responsibilities
- Support operations on all GMP manufacturing systems in the Manufacturing Facilities in Devens, MA
- Lead and participate in automation engineering initiatives for manufacturing operations, system enhancements, and site expansion activities for Clinical manufacturing and Biologics development operations
- Design, configure, integrate, and test process control systems
- Participate in cross-functional teams to develop 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 procedures
- 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
- Collaborate with Validation, Quality, Manufacturing Engineering, and Manufacturing operations to keep site operations functional
Required Qualifications
- BS in Chemical Engineering, Electrical Engineering, or 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 in executing Factory Acceptance Tests and 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
Preferred Qualifications
- Experience on Manufacturing Execution System (Syncade)
- Experience on OSI PI data historian applications
- Experience on automation validation (DeltaV, MES, PI) in GMP environment including test script generation and execution
- Ability to troubleshoot control systems from field element up through operator interfaces and databases
- Ability to work with visual basics scripting
Skills Required
- Strong interpersonal skills and ability to work in a team environment
- Strong communication skills including oral and formal presentations
- Ability to work in a fast-paced multi-tasking environment
- Ability to work independently
Benefits & Perks
- 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
- Summer hours flexibility
Locations
- Devens MA, United States
Salary
Estimated Salary Rangemedium confidence
120,000 - 180,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Strong interpersonal skills and ability to work in a team environmentintermediate
- Strong communication skills including oral and formal presentationsintermediate
- Ability to work in a fast-paced multi-tasking environmentintermediate
- Ability to work independentlyintermediate
Required Qualifications
- BS in Chemical Engineering, Electrical Engineering, or related equivalent engineering field (experience)
- Minimum 9 years of industry experience on DeltaV distributed control systems (experience)
- Minimum of 2 years of experience in Pharmaceutical or Biotechnology industries (experience)
- In-depth understanding of ISA S88 and batch processing operations (experience)
- Experience in executing Factory Acceptance Tests and supporting commissioning activities (hardware loop checks, cabinet testing) (experience)
- Experience on change control management, deviation logs, and investigation under FDA regulated environment (experience)
- Understanding of engineering documentation such as P&IDs, Process Flow diagrams, and standard operating procedures (experience)
Preferred Qualifications
- Experience on Manufacturing Execution System (Syncade) (experience)
- Experience on OSI PI data historian applications (experience)
- Experience on automation validation (DeltaV, MES, PI) in GMP environment including test script generation and execution (experience)
- Ability to troubleshoot control systems from field element up through operator interfaces and databases (experience)
- Ability to work with visual basics scripting (experience)
Responsibilities
- Support operations on all GMP manufacturing systems in the Manufacturing Facilities in Devens, MA
- Lead and participate in automation engineering initiatives for manufacturing operations, system enhancements, and site expansion activities for Clinical manufacturing and Biologics development operations
- Design, configure, integrate, and test process control systems
- Participate in cross-functional teams to develop 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 procedures
- 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
- Collaborate with Validation, Quality, Manufacturing Engineering, and Manufacturing operations to keep site operations functional
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
Tags & Categories
Answer 10 quick questions to check your fit for Senior Automation Engineer (DeltaV) @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs