Associate Director, Technical Operations (drug Substance)

539

Wilmington, DE, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
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8+ years cgmp biological or pharma experience
Lead engineering design firms for drug substance
Execute fat, sat, iq/oq qualification activities
** The job posting is for an Associate Director of Technical Operations in Wilmington, DE, focusing on the manufacturing and technical aspects of drug substance operations at a new antibody drug conjugate facility. The ideal candidate should have extensive experience in a cGMP biotech environment, with strong leadership and technical skills to oversee the build and operation of the facility. **

Job Summary

  • Join the launch of a cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware to transform cancer care.
  • The role provides comprehensive technical leadership for the Drug Substance organization from design through commercial operation.
  • 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: 75

** The job posting is for an Associate Director of Technical Operations in Wilmington, DE, focusing on the manufacturing and technical aspects of drug substance operations at a new antibody drug conjugate facility. The ideal candidate should have extensive experience in a cGMP biotech environment, with strong leadership and technical skills to oversee the build and operation of the facility. **

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 experience
  • Lead engineering design firms for drug substance
  • Execute FAT, SAT, IQ/OQ qualification activities
  • Manage process hazard and quality risk assessments
  • Oversee engineering batches and PPQ runs

Nice-to-have

  • Start-up experience in commercial DS facility
  • Hands-on ADC manufacturing expertise
  • Six Sigma continuous improvement skills
  • FMEA risk-based manufacturing approach
  • Cross-cultural awareness and teamwork

Key Requirements

  • Bachelor's degree in engineering or science
  • Minimum 8 years in cGMP biological/vaccine/pharma facility
  • Experience with antibody drug conjugates preferred
  • Expertise in chromatography and TFF operations advantageous

Work Rights

Not specified

Tailored Resume

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