Senior Specialist, Drug Product Operations - Wilmington Biotech

539

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: elig...
Hybrid
Cgmp biological/vaccine/pharma facility
Aseptic manufacturing experience
Drug product operations
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.
  • The Manufacturing Senior Specialist will play a pivotal role in ensuring smooth operation of various aspects of manufacturing and provide comprehensive manufacturing and technical leadership to the drug product organization.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits.

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/pharma facility
  • aseptic manufacturing experience
  • drug product operations
  • technical leadership
  • sterile supply, formulation, filling

Nice-to-have

  • data driven approach
  • risk-based approach
  • adapt to changing priorities
  • inclusive environment
  • purpose-driven science

Key Requirements

  • Bachelor’s degree in engineering, science or related discipline
  • Five or more (5+) years working in a cGMP facility
  • Start-up experience in a large-scale commercial drug product facility highly desirable
  • Ability to operate within a matrix team
  • Experience with AVI/MVI and creation of library of defects
  • 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