Principal Scientist, Mixed Modalities, Sterile Product Development

Memorialdrivevetclinic

$169,700.00 - $267,200.00; bonus + long-term incen...
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Parenteral drug product development
Sterile injectable, implantable, ophthalmic, inhaled dosage forms
Formulation and process development
** Memorialdrivevetclinic is seeking a Principal Scientist specializing in Mixed Modalities for Sterile Product Development. The role focuses on developing parenteral dosage forms and requires extensive experience in drug product development, leadership, and collaboration within multidisciplinary teams. **

Job Summary

  • The Mixed Modalities team develops parenteral dosage forms for small, intermediate, and large molecules from preclinical studies to commercialization, ensuring robust composition, packaging, and scalable processes.
  • The Principal Scientist will provide strategic and technical leadership on program development teams, supporting early and late-stage candidates, and collaborating across functions to drive milestones.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement, paid holidays, and vacation.

Matching Summary

Match Score: 75

** Memorialdrivevetclinic is seeking a Principal Scientist specializing in Mixed Modalities for Sterile Product Development. The role focuses on developing parenteral dosage forms and requires extensive experience in drug product development, leadership, and collaboration within multidisciplinary teams. **

Salary

$169,700.00 - $267,200.00; Bonus and long-term incentive eligibility; Comprehensive benefits package

Skills & Requirements

Must-have

  • Parenteral drug product development
  • Sterile injectable, implantable, ophthalmic, inhaled dosage forms
  • Formulation and process development
  • Quality by Design principles
  • Process scale-up and technology transfer
  • Regulatory filings and CMC requirements

Nice-to-have

  • Cross-functional team leadership
  • Mentorship of junior scientists
  • External academic and regulatory community engagement
  • Innovation and strategic objective championing

Key Requirements

  • Ph.D. with 8+ years industry experience
  • M.S. with 10+ years industry experience
  • B.S. with 14+ years industry experience
  • Experience in parenteral formulation and process development
  • Experience with QbD principles and DOE studies
  • Experience authoring regulatory filings
  • Experience leading cross-functional teams

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter