Senior Specialist, Manufacturing Automation Engineer (on-site)

Newyorkbioconnect

Rahway, NJ, US
Base: $106,200 - $167,200; bonus/equity: eligible ...
Hybrid
Deltav and plc system programming
Gmp manufacturing environment experience
Automation system design and commissioning
The Senior Specialist – Manufacturing Automation will be a key member of the MACS Center automation team supporting a new multi-modality GMP clinical manufacturing plant in Rahway, New Jersey

Job Summary

  • The Senior Specialist – Manufacturing Automation will be a key member of the MACS Center automation team supporting a new multi-modality GMP clinical manufacturing plant in Rahway, New Jersey.
  • This role involves collaboration with development engineers, compliance representatives, and operations to ensure reliable and compliant automation solutions across multiple facilities.
  • The company offers a comprehensive benefits package and supports a hybrid work model for office-based positions, with a salary range of $106,200 to $167,200 plus bonus and long-term incentives.

Matching Summary

The Senior Specialist – Manufacturing Automation will be a key member of the MACS Center automation team supporting a new multi-modality GMP clinical manufacturing plant in Rahway, New Jersey.

Salary

Base: $106,200 - $167,200; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays and more

Skills & Requirements

Must-have

  • DeltaV and PLC system programming
  • GMP manufacturing environment experience
  • Automation system design and commissioning
  • Root cause analysis and troubleshooting
  • Project management and team leadership
  • Compliance and change management support

Nice-to-have

  • Technical mentorship and training
  • Experience with wireless and OPC interfaces
  • Networking and IT integration skills
  • Innovation and creativity in automation
  • Strong communication and organizational skills

Key Requirements

  • Bachelor’s degree with 8 years experience or Master’s with 5 years
  • Pharmaceutical GMP pilot plant or manufacturing experience
  • Experience with DeltaV and Rockwell PLC systems
  • Knowledge of US and EU GMP and safety regulations
  • Project management experience
  • Ability to prepare SOP and GMP documentation
  • US work authorization required

Work Rights

US and Puerto Rico Residents Only

Sponsorship: available

Tailored Resume

Cover Letter