Associate Principal Scientist, Engineering- Biologics, Sterile Drug Product Commercialization

Mayoly

$142,400.00 - $224,100.00; bonus/equity: annual bo...
Hybrid (3 days on-site, 1 day remote)
Biologics drug product process development
Sterile drug product manufacturing
Process scale up and technology transfer
Mayoly is seeking an Associate Principal Scientist for their Sterile Drug Product Commercialization group, focusing on the commercialization of biologics. The ideal candidate will have a strong background in drug product process development, with responsibilities spanning from process characterization to regulatory submission

Job Summary

  • The Sterile Drug Product Commercialization group provides technical process leadership and laboratory capabilities for late stage and commercial drug product processes for biologics and combination products.
  • The Associate Principal Scientist will have a key focus on driving excellence in process characterization, scale up, transfer and process validation activities.
  • The company offers 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: 85

Mayoly is seeking an Associate Principal Scientist for their Sterile Drug Product Commercialization group, focusing on the commercialization of biologics. The ideal candidate will have a strong background in drug product process development, with responsibilities spanning from process characterization to regulatory submission.

Salary

$142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, and sick days

Skills & Requirements

Must-have

  • Biologics drug product process development
  • Sterile drug product manufacturing
  • Process scale up and technology transfer
  • Process validation and characterization
  • Regulatory submissions support

Nice-to-have

  • High performance culture
  • Out of the box thinking
  • Innovation and learning
  • Diversity and inclusion

Key Requirements

  • BS with 10 years experience or MS with 8 years experience or PhD with 4 years experience
  • Experience with biologics drug product manufacturing
  • Technical expertise in sterile drug product fill finish
  • Experience with technology transfer and scale-up
  • Working knowledge of cGMPs and ICH Quality norms

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter