Specialist, Automation Engineering (onsite)

Laboratory Animal Management Association

Rahway, New Jersey, USA
Base: $87,300.00 - $137,400.00; bonus/equity: annu...
3 days onsite, 1 day remote
Cgmp
Process automation
Ot/it systems
The Laboratory Animal Management Association is seeking a Specialist in Automation Engineering for their FLEx Center in Rahway, New Jersey. This onsite role focuses on supporting the automation systems crucial for sterile clinical manufacturing processes and requires a strong background in cGMP principles, automation technologies, and project management

Job Summary

  • The Specialist, Automation Engineering role will provide end-to-end automation engineering support for the Rahway, NJ FLEx Center, with a primary focus on sterile clinical manufacturing within Pharmaceutical Sciences and Clinical Supply (PSCS), Pharmaceutical Operations Engineering (Pharm Ops Engineering).
  • This position supports start-up operations and new capital investments in the clinical supply area, including automation lifecycle management, data and analytics, and site representation on capital projects.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and a comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 85

The Laboratory Animal Management Association is seeking a Specialist in Automation Engineering for their FLEx Center in Rahway, New Jersey. This onsite role focuses on supporting the automation systems crucial for sterile clinical manufacturing processes and requires a strong background in cGMP principles, automation technologies, and project management.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • cGMP
  • process automation
  • OT/IT systems
  • sterile clinical manufacturing
  • automation lifecycle management
  • data integrity
  • cybersecurity

Nice-to-have

  • lean and continuous improvement principles
  • cross-functional teams
  • independent ownership
  • prioritization and delivery
  • fast-paced clinical manufacturing

Key Requirements

  • Bachelor’s degree in Engineering, Science, Information Technology, or related field
  • Minimum 2 years of experience in process automation
  • Strong knowledge of cGMP, Quality Systems, Safety, Environmental, data integrity, and validation principles
  • Hands-on experience maintaining validated automation systems
  • Proficiency with PLC/SCADA and industrial networking fundamentals

Work Rights

Not specified

Tailored Resume

Cover Letter