Senior Specialist, Drug Product Operations - Wilmington Biotech

39med

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: elig...
Hybrid
Cgmp biological/vaccine/pharma facility
Aseptic manufacturing experience
Drug product manufacturing
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; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, and sick days.

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: Comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • cGMP biological/vaccine/pharma facility
  • aseptic manufacturing experience
  • drug product manufacturing
  • sterile supply, formulation, filling, lyophilization
  • process hazard analyses
  • quality risk assessments
  • equipment qualification (IQ/OQ)

Nice-to-have

  • start-up experience
  • data driven approach
  • risk-based approach
  • adapt to changing priorities
  • inclusive environment
  • respectfully challenge thinking

Key Requirements

  • 5+ years cGMP biological/vaccine/pharma facility
  • Bachelor’s degree in engineering, science or related discipline
  • Experience with AVI/MVI and creation of library of defects
  • Experience with CQV activities
  • Experience with Six Sigma
  • Experience with FMEA
  • Understanding of USP1790 and Annex 1

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter