Principal Scientist, Mixed Modalities, Sterile Product Development

Drugdiscovery

Base: $169,700.00 - $267,200.00; bonus/equity: ann...
Hybrid
Parenteral drug product development
Sterile product formulation
Process development and scale-up
The Mixed Modalities team develops parenteral dosage forms for small, intermediate, and large molecules from preclinical toxicology studies to commercialization

Job Summary

  • The Mixed Modalities team develops parenteral dosage forms for small, intermediate, and large molecules from preclinical toxicology studies to commercialization.
  • The successful candidate will provide strategic and technical leadership on program development teams, driving defined milestones and collaborating across functions.
  • The company offers a comprehensive package of benefits including medical, dental, vision healthcare, retirement benefits, paid holidays, and vacation.

Matching Summary

The Mixed Modalities team develops parenteral dosage forms for small, intermediate, and large molecules from preclinical toxicology studies to commercialization.

Salary

Base: $169,700.00 - $267,200.00; 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

  • parenteral drug product development
  • sterile product formulation
  • process development and scale-up
  • drug product composition
  • primary packaging development
  • regulatory filings support

Nice-to-have

  • cross-functional team leadership
  • external academic community networking
  • mentorship of junior scientists
  • innovative thinking and problem solving

Key Requirements

  • Ph.D. with 8+ years industry experience
  • M.S. with 10+ years industry experience
  • B.S. with 14+ years industry experience
  • cGMP industrial background
  • experience with parenteral formulation and process development
  • experience with QbD principles and DOE studies
  • experience with process scale-up and technology transfer
  • experience authoring regulatory filings
  • working knowledge of FDA, ICH, and regulatory requirements

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter