Associate Director, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (onsite)

Merck & Co., Inc., Rahway, NJ, USA

Rahway, New Jersey, USA
Base: $142,400.00 - $224,100.00; bonus/equity: eli...
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Oral solid dosage manufacturing
Gmp documentation review and approval
Process robustness assessments
** Merck & Co., Inc. is seeking an Associate Director of Process Engineering for its Oral Solid Dosage team in Rahway, NJ. The role requires extensive experience in GMP manufacturing and process engineering, focusing on leading clinical supply manufacturing and mentoring a team to ensure the quality and efficiency of drug products. **

Job Summary

  • The Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products, leveraging pharmaceutical unit operations.
  • Lead and strategically plan on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.
  • We offer 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: 75

** Merck & Co., Inc. is seeking an Associate Director of Process Engineering for its Oral Solid Dosage team in Rahway, NJ. The role requires extensive experience in GMP manufacturing and process engineering, focusing on leading clinical supply manufacturing and mentoring a team to ensure the quality and efficiency of drug products. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: 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

  • Oral Solid Dosage manufacturing
  • GMP documentation review and approval
  • Process robustness assessments
  • Root cause analysis
  • cGMP, FDA, EMA regulatory requirements
  • Small molecule drug product processing

Nice-to-have

  • Subject matter expert in drug delivery
  • Experience in Formulation and Analytical Sciences
  • Knowledge of Clinical Supply Chain Operations
  • Foster culture of collaboration and innovation
  • Hands-on optimization of existing technologies

Key Requirements

  • Minimum 10 years relevant experience with BS
  • Minimum 8 years relevant experience with MS
  • Minimum 4 years relevant experience with PhD
  • Experience leading GMP manufacturing facilities
  • Experience managing and developing teams

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter