Senior Specialist, Drug Product Operations - Wilmington Biotech

microsatsystems.biz

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: elig...
Hybrid
Cgmp biological/vaccine/pharma facility experience
Aseptic manufacturing experience
Engineering design firm engagement
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 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, compassionate and sick days

Skills & Requirements

Must-have

  • cGMP biological/vaccine/pharma facility experience
  • Aseptic manufacturing experience
  • Engineering design firm engagement
  • Technical documentation creation/revision
  • Sterile supply and formulation expertise
  • Isolator and filling line operation
  • Lyophilization and capping processes
  • Visual inspection (manual/automated)

Nice-to-have

  • Safety First, Quality Always mindset
  • Inclusion for all culture
  • Right First Time Culture promotion
  • Data driven root cause analysis
  • Risk-based manufacturing approach
  • Adaptability to changing priorities

Key Requirements

  • 5+ years cGMP biological/vaccine/pharma facility experience
  • Bachelor’s degree in engineering/science
  • Start-up experience in large-scale commercial drug product facility
  • Experience with AVI/MVI and defect library creation
  • Experience with CQV activities
  • Experience with Six Sigma / Lean Six Sigma

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter