Senior Specialist, Manufacturing Automation Engineer (on-site)

39med

Rahway, NJ, USA
Base: $106,200.00 - $167,200.00; bonus/equity: ann...
Hybrid (3 days on-site, 1 day remote)
Gmp pilot plant operations experience
Deltav or rockwell plc programming
Automation system design and qualification
39med is seeking a Senior Specialist, Manufacturing Automation Engineer to join their Enabling Facilities group in Rahway, NJ. The role involves significant technical and project management responsibilities in automation for a new multi-modality drug substance development and GMP clinical manufacturing plant

Job Summary

  • The role serves as a technical subject matter expert supporting the Modality Agnostic Chemistry Scaleup Center in Rahway, New Jersey.
  • Candidates will lead automation equipment design, system commissioning, and qualification activities for new GMP manufacturing facilities.
  • The position offers a comprehensive benefits package including medical, dental, vision, 401(k), and potential annual bonuses.

Matching Summary

Match Score: 85

39med is seeking a Senior Specialist, Manufacturing Automation Engineer to join their Enabling Facilities group in Rahway, NJ. The role involves significant technical and project management responsibilities in automation for a new multi-modality drug substance development and GMP clinical manufacturing plant.

Salary

Base: $106,200.00 - $167,200.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays

Skills & Requirements

Must-have

  • GMP Pilot Plant Operations experience
  • DeltaV or Rockwell PLC programming
  • Automation system design and qualification
  • Root cause analysis and troubleshooting
  • Capital project management direction

Nice-to-have

  • PID tuning of instrumentation loops
  • Wireless technologies and Charms I/O
  • Technical mentorship of engineers
  • Process Hazard Analysis (PHA) knowledge
  • Object-oriented programming languages

Key Requirements

  • Bachelor's degree with 8 years experience or Master's with 5 years
  • Pharmaceutical GMP manufacturing environment experience
  • US work authorization required (Visa sponsorship available)

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter