Associate Director, Technical Operations (drug Substance)

Merck & Co., Inc.

Wilmington, DE, US
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days on-site, 1 day remote)
8+ years cgmp biological or pharma facility experience
Leading fat sat iq oq engineering batches
Process hazard analysis and quality risk assessments
Merck & Co., Inc. is seeking an Associate Director of Technical Operations for their new Antibody Drug Conjugate manufacturing facility in Wilmington, DE. The position requires extensive experience in pharmaceutical manufacturing and offers a hybrid work model along with a comprehensive benefits package

Job Summary

  • The role involves leading the design, commissioning, and operation of a cutting-edge Antibody Drug Conjugate manufacturing facility in Wilmington, Delaware.
  • Candidates will provide comprehensive technical leadership on manufacturing processes including conjugation, chromatography, and filling while ensuring GMP compliance.
  • The position offers a competitive salary range of $142,400 to $224,100 along with medical, dental, vision, and retirement benefits.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking an Associate Director of Technical Operations for their new Antibody Drug Conjugate manufacturing facility in Wilmington, DE. The position requires extensive experience in pharmaceutical manufacturing and offers a hybrid work model along with a comprehensive benefits package.

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

Skills & Requirements

Must-have

  • 8+ years cGMP biological or pharma facility experience
  • Leading FAT SAT IQ OQ engineering batches
  • Process Hazard Analysis and Quality Risk Assessments
  • Technical leadership in chromatography and TFF
  • Experience with PPQ runs and tech transfer

Nice-to-have

  • Start-up experience in large-scale commercial DS facility
  • Hands-on experience with antibody drug conjugates
  • Six Sigma data driven root cause analysis
  • Risk-based manufacturing using FMEA tools
  • Cross-cultural awareness and team collaboration

Key Requirements

  • Bachelor's degree in engineering or science
  • Eight or more years in cGMP biological/pharma facility
  • No visa sponsorship available

Work Rights

Not specified

Tailored Resume

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