Senior Specialist, Drug Product Operations - Wilmington Biotech

Imsapharma Com Ar

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: elig...
Hybrid
Cgmp biological/vaccine/pharma facility experience
Aseptic manufacturing experience
Drug product operations
We are launching a cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware, to transform cancer care through innovation and collaboration

Job Summary

  • We are launching a cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware, to transform cancer care through innovation and collaboration.
  • This role offers the chance to contribute to site development and ensure successful GMP manufacturing, providing comprehensive manufacturing and technical leadership to the drug product organization.
  • The company offers a comprehensive package of benefits including medical, dental, vision, retirement benefits, paid holidays, vacation, and compassionate and sick days.

Matching Summary

We are launching a cutting-edge Antibody Drug Conjugate (ADC) manufacturing facility in Wilmington, Delaware, to transform cancer care through innovation and collaboration.

Salary

Base: $94,300.00 - $148,500.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: comprehensive package of benefits

Skills & Requirements

Must-have

  • cGMP biological/vaccine/pharma facility experience
  • aseptic manufacturing experience
  • drug product operations
  • manufacturing and technical leadership
  • sterile supply, formulation, filling, lyophilization
  • cGMP compliance
  • risk-based approach to manufacturing

Nice-to-have

  • start-up experience
  • data driven approach
  • lean six sigma continuous improvement
  • collaboration and purpose-driven science
  • inclusive environment
  • respectfully challenge thinking

Key Requirements

  • 5+ years cGMP biological, vaccine or pharma facility experience
  • Bachelor’s degree in engineering, science or related discipline
  • Prior aseptic manufacturing experience preferred
  • Start-up experience in large-scale commercial drug product facility highly desirable
  • Experience with AVI/MVI and creation of library of defects
  • Understanding of USP1790 and Annex 1

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter