Associate Director, Engineering

Merck & Co., Inc.

Rahway, NJ, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid
Gmp clinical supply facility experience
Equipment start-up and qualification
Small molecule drug substance process development
The Associate Director will build and lead a team of 5-10 engineers to support the MACS Center, a new potent, multi-modality drug substance development and GMP clinical manufacturing plant in Rahway, New Jersey

Job Summary

  • The Associate Director will build and lead a team of 5-10 engineers to support the MACS Center, a new potent, multi-modality drug substance development and GMP clinical manufacturing plant in Rahway, New Jersey.
  • This role requires establishing requirements for the first-of-a-kind facility by the ready for science target date of 2Q 2027 while contributing to equipment design, system commissioning, and qualification.
  • The successful candidate will be eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

The Associate Director will build and lead a team of 5-10 engineers to support the MACS Center, a new potent, multi-modality drug substance development and GMP clinical manufacturing plant in Rahway, New Jersey.

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • GMP clinical supply facility experience
  • Equipment start-up and qualification
  • Small molecule drug substance process development
  • Leading compliance investigations and change management
  • Process Hazard Analysis (PHA) and LOPA
  • Building high performance engineering teams

Nice-to-have

  • GMP facility design and commissioning experience
  • Potent compound processing and containment systems
  • Experience with automation systems like DeltaV or PLC
  • Managing matrix teams and direct reports
  • Fostering culture of collaboration and innovation

Key Requirements

  • Bachelor's degree with 8 years experience or Master's with 7 years or PhD with 5 years
  • Experience in GMP clinical supply facility operations
  • Experience with equipment start-up and qualification
  • Ability to convert process needs to executable procedures
  • Visa sponsorship available for qualified candidates

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter