Senior Specialist, Drug Product Operations - Wilmington Biotech

medhunter.de

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: annu...
Hybrid
Cgmp biological, vaccine or pharma facility
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 salary range for this role is $94,300.00 - $148,500.00

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 or pharma facility
  • aseptic manufacturing experience
  • engineering design firm engagement
  • Process Hazard Analyses
  • Quality Risk Assessments
  • equipment qualification deliverables

Nice-to-have

  • Safety First, Quality Always mindset
  • Right First Time Culture
  • data driven approach
  • risk-based approach to manufacturing

Key Requirements

  • Five or more (5+) years working in a cGMP biological, vaccine or pharma facility
  • Bachelor’s degree in engineering, science or related discipline
  • Start-up experience in a large-scale commercial drug product facility highly desirable
  • Previous experience with CQV activities will be advantageous

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter