Senior Specialist, Drug Product Operations - Wilmington Biotech

29

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: elig...
Hybrid
Cgmp biological, vaccine or pharma facility
Aseptic manufacturing experience
Sterile supply, formulation, filling
We’re thrilled to announce the launch of our cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware—a bold step forward in transforming cancer care through innovation, collaboration, and purpose-driven science

Job Summary

  • We’re thrilled to announce the launch of our cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware—a bold step forward in transforming cancer care through innovation, collaboration, and purpose-driven science.
  • In this position the Manufacturing Senior Specialist will play a pivotal role in ensuring smooth operation of various aspects of manufacturing.
  • The salary range for this role is $94,300.00 - $148,500.00

Matching Summary

We’re thrilled to announce the launch of our cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware—a bold step forward in transforming cancer care through innovation, collaboration, and purpose-driven science.

Salary

Base: $94,300.00 - $148,500.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: medical, dental, vision healthcare and other insurance benefits, retirement benefits, 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • cGMP biological, vaccine or pharma facility
  • aseptic manufacturing experience
  • sterile supply, formulation, filling
  • isolators, lyophilization, visual inspection
  • engineering design firm engagement
  • process hazard analyses, quality risk assessments
  • factory acceptance testing, site acceptance testing

Nice-to-have

  • data driven approach to root cause analysis
  • risk-based approach to manufacturing
  • adapt to changing priorities
  • inclusive environment
  • respectfully challenge thinking

Key Requirements

  • 5+ years cGMP experience
  • Bachelor’s degree in engineering, science or related discipline
  • Start-up experience in large-scale commercial drug product facility
  • experience with AVI/MVI and creation of library of defects
  • experience with CQV activities
  • experience in data driven approach to root cause analysis
  • experience in a risk-based approach to manufacturing

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter