Senior Specialist, Drug Product Operations - Wilmington Biotech

Laboratory Animal Management Association

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: annu...
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.
  • 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: Annual bonus and long-term incentive, if applicable; Benefits: 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
  • high-potency manufacturing
  • process hazard analysis
  • quality risk assessment

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
  • Ability to operate within a matrix team
  • Previous experience manufacturing/technical support
  • Experience with AVI/MVI and library of defects
  • Experience with CQV activities
  • Experience in data driven root cause analysis
  • Experience in risk-based approach
  • Understanding of USP1790 and Annex 1

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter