Associate Director, Technical Operations (drug Substance)

Merck & Co., Inc.

Wilmington, DE, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
8+ years cgmp biological or pharma experience
Leadership in fat, sat, iq/oq activities
Experience with engineering batches and ppq runs
Merck & Co., Inc. is seeking an Associate Director of Technical Operations for its new Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, DE. The role involves providing technical leadership in drug substance manufacturing, ensuring oversight of engineering design, and contributing to the launch of innovative cancer therapies

Job Summary

  • This role offers the opportunity to join a cutting-edge Antibody Drug Conjugate manufacturing facility launch in Wilmington, Delaware.
  • The successful candidate will provide comprehensive manufacturing leadership from design through operation, including leading process hazard analyses and equipment qualification.
  • Employees are eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and 401(k) retirement plans.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking an Associate Director of Technical Operations for its new Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, DE. The role involves providing technical leadership in drug substance manufacturing, ensuring oversight of engineering design, and contributing to the launch of innovative cancer therapies.

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

  • 8+ years cGMP biological or pharma experience
  • Leadership in FAT, SAT, IQ/OQ activities
  • Experience with engineering batches and PPQ runs
  • Technical expertise in chromatography and TFF
  • Ability to lead matrix teams on floor activities

Nice-to-have

  • Start-up experience in commercial drug substance facility
  • Hands-on experience with antibody drug conjugates
  • Six Sigma data-driven root cause analysis skills
  • Risk-based manufacturing approach using FMEA tools

Key Requirements

  • Bachelor's degree in engineering or science
  • Minimum 8 years in cGMP biological/vaccine/pharma facility
  • No visa sponsorship available

Work Rights

Not specified

Tailored Resume

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