Senior Specialist, Drug Product Operations - Wilmington Biotech

vetshired.us

Wilmington, Delaware, US
Base: $94,300.00 - $148,500.00; bonus/equity: elig...
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Cgmp biological, vaccine or pharma facility
Aseptic manufacturing experience
Factory acceptance testing (fat)
** The Senior Specialist in Drug Product Operations at Merck's new Wilmington Biotech facility focuses on the manufacturing of Antibody Drug Conjugates (ADCs) to advance cancer care. The role involves technical leadership in GMP manufacturing processes, ensuring compliance, and supporting product launches, while fostering a culture of safety and innovation. **

Job Summary

  • This role offers you the chance to contribute to the site's development and ensure successful GMP manufacturing.
  • In partnership with site MS&T the Manufacturing Senior Specialist will provide comprehensive manufacturing and technical leadership to the drug product organization.
  • We offer a comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 75

** The Senior Specialist in Drug Product Operations at Merck's new Wilmington Biotech facility focuses on the manufacturing of Antibody Drug Conjugates (ADCs) to advance cancer care. The role involves technical leadership in GMP manufacturing processes, ensuring compliance, and supporting product launches, while fostering a culture of safety and innovation. **

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 (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
  • factory acceptance testing (FAT)
  • site acceptance testing (SAT)
  • equipment qualification deliverables
  • manufacturing batch records
  • sterile supply, formulation, filling, lyophilization

Nice-to-have

  • data driven approach to root cause analysis
  • risk-based approach to manufacturing
  • culture of excellence, inclusion, and impact
  • Right First Time Culture
  • AI-driven antibody optimization

Key Requirements

  • 5+ years cGMP biological, vaccine or pharma facility
  • Bachelor’s degree in engineering, science or related discipline
  • Start-up experience in large-scale commercial drug product facility
  • CQV activities experience
  • US and Puerto Rico Residents Only

Work Rights

Not specified

Sponsorship: available

Tailored Resume

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