Senior Automation Engineer — Radiopharma Manufacturing

Bristol-Myers Squibb Company

Guam

On-site

USD 108,000 - 131,000

Full time

5 days ago
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Benefits offered by this job

Wellbeing support
Retirement plan and financial security
Insurance offerings (medical, dental,視
Flexible Time Off
Holidays: 11 company holidays

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Senior Automation/Controls Engineer to support clinical and commercial manufacturing at Indianapolis sites. You will design, develop, and support automation and control systems for radiopharmaceutical processes, ensure GMP compliance, and mentor junior staff.

You will collaborate with engineering, production, and quality teams, lead deviation investigations, CAPA efforts, and work with external vendors to implement robust

Qualifications

  • BS in Electrical, Mechanical, Automation, or related engineering field.
  • MS or advanced degree preferred.
  • 7+ years in automation/control engineering in pharma/regulated manufacturing.

Responsibilities

  • Maintain and operate automation/control systems for radiopharmaceutical manufacturing.
  • Lead development and lifecycle management of automation systems.
  • Support GMP operations including deviation investigations, CAPA, and change control.
  • Architect and implement PLC/SCADA/HMI platforms for expansion and manufacturing needs.
  • Ensure regulatory and GMP compliance and mentor junior engineers.

Skills

Automation design
PLC programming (Rockwell/Siemens)
SCADA/HMI development
Cognex vision systems
Robotics
Process instrumentation
IT infrastructure knowledge
Leadership

Education

BS in Electrical/Mechanical/Automation Engineering
MS preferred

Tools

Rockwell/Siemens PLCs
SCADA/HMI tools
Cognex vision
Robotics systems
Data historian systems

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Senior Automation/Controls Engineer to support clinical and commercial manufacturing at Indianapolis sites. You will design, develop, and support automation and control systems for radiopharmaceutical processes, ensure GMP compliance, and mentor junior staff.

You will collaborate with engineering, production, and quality teams, lead deviation investigations, CAPA efforts, and work with external vendors to implement robust

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