Director Of Gmp Site Operations, Small Molecule Ar&d

Merck & Co., Inc.

Rahway, NJ, USA
Base: $173,200.00 - $272,600.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Gmp compliance oversight
Cleaning verification experience
Solvent release management
Merck & Co., Inc. is seeking a Director of GMP Site Operations in Rahway, NJ, to lead a team in supporting GMP analytical activities for drug substance and product development. The ideal candidate should possess extensive industry experience in pharmaceutical development, particularly in GMP compliance and operational excellence

Job Summary

  • The Director will lead a team of specialists and scientists supporting GMP analytical activities including cleaning verification and solvent release.
  • This role requires ensuring cGMP compliance, maintaining inspection readiness, and providing technical oversight on lab investigations.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement plans, and paid holidays.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Director of GMP Site Operations in Rahway, NJ, to lead a team in supporting GMP analytical activities for drug substance and product development. The ideal candidate should possess extensive industry experience in pharmaceutical development, particularly in GMP compliance and operational excellence.

Salary

Base: $173,200.00 - $272,600.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • GMP compliance oversight
  • Cleaning verification experience
  • Solvent release management
  • In-process testing leadership
  • Team recruitment and development

Nice-to-have

  • Lab investigations and deviations expertise
  • Internal and external audit support
  • Process improvement initiatives
  • Strategic cultural initiative driving
  • Cross-functional collaboration skills

Key Requirements

  • BS or MS in Chemistry with 10+ years industry experience
  • PhD in Chemistry with 7+ years industry experience
  • Experience managing GMP analytical labs
  • Knowledge of FDA guidelines and ICH standards

Work Rights

Not specified

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