Associate Director, Technical Operations (drug Substance)

29

Wilmington, DE, US
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days onsite per week, monday - thursday, with fridays remote)
8+ years cgmp biological facility experience
Lead engineering design firms for drug substance
Execute fat sat iq oq qualification activities
The Associate Director of Technical Operations at Company 29 in Wilmington, DE, is a leadership role focused on overseeing drug substance manufacturing processes in a new Antibody Drug Conjugate (ADC) facility. The position requires extensive experience in cGMP settings and technical expertise in drug substance manufacturing, while promoting a culture of innovation and collaboration

Job Summary

  • Join the launch of a cutting-edge Antibody Drug Conjugate manufacturing facility in Wilmington, Delaware to transform cancer care.
  • The role provides comprehensive manufacturing and technical leadership from design through operation, including overseeing engineering batches and PPQ runs.
  • Candidates will receive a competitive salary range of $142,400.00 - $224,100.00 along with medical, dental, vision, and retirement benefits.

Matching Summary

Match Score: 85

The Associate Director of Technical Operations at Company 29 in Wilmington, DE, is a leadership role focused on overseeing drug substance manufacturing processes in a new Antibody Drug Conjugate (ADC) facility. The position requires extensive experience in cGMP settings and technical expertise in drug substance manufacturing, while promoting a culture of innovation and collaboration.

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 facility experience
  • Lead engineering design firms for drug substance
  • Execute FAT SAT IQ OQ qualification activities
  • Manage process hazard and quality risk assessments
  • Oversee equipment commissioning and technical documentation

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
  • FMEA risk-based manufacturing approach expertise
  • Cross-cultural awareness and team collaboration

Key Requirements

  • Bachelor's degree in engineering or science
  • Eight or more years in cGMP pharmaceutical facility
  • Experience with antibody drug conjugates preferred
  • No visa sponsorship available

Work Rights

Not specified

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