Principal Scientist, Mixed Modalities, Sterile Product Development

Vetamc

Unknown
Base: $169,700.00 - $267,200.00; bonus/equity: eli...
Hybrid
Parenteral formulation and process development
Cgmp industrial background
Drug product composition and process 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, collaborate across functions, and mentor a small group of scientists.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, vacation, and sick days.

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: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive medical, dental, vision, retirement, paid holidays, vacation, and sick days

Skills & Requirements

Must-have

  • Parenteral formulation and process development
  • cGMP industrial background
  • Drug product composition and process scale-up
  • Regulatory filings and compliance
  • Cross-functional team leadership
  • Quality by Design (QbD) application
  • Mentorship of junior scientists

Nice-to-have

  • Experience with intermediate modalities
  • Alternate delivery technologies knowledge
  • Influencing global regulatory strategies
  • Large capital project team experience
  • Strong interpersonal and collaboration skills
  • Innovative thinking and initiative
  • Professional networking

Key Requirements

  • Ph.D. with 8+ years industry experience or equivalent
  • Experience developing sterile products for IV, IM, and/or SC routes
  • Strong knowledge of FDA, ICH, and regulatory requirements
  • Experience with process scale-up and technology transfer
  • Demonstrated scientific leadership and publication record
  • Ability to work in a fast-paced multidisciplinary environment
  • U.S. work authorization required

Work Rights

US and Puerto Rico Residents Only

Sponsorship: available

Tailored Resume

Cover Letter