Principal Scientist, Mixed Modalities, Sterile Product Development

Imsapharma Com Ar

$169,700.00 - $267,200.00; bonus/equity: annual bo...
Hybrid (3 days onsite, 1 day remote)
Sterile product development
Parenteral drug product development
Formulation and process development
Imsapharma Com Ar is seeking a Principal Scientist in Mixed Modalities for Sterile Product Development, responsible for the development of parenteral dosage forms. The ideal candidate will have significant experience in formulation science, leadership, and regulatory processes within a hybrid work environment

Job Summary

  • The Mixed Modalities team develops parenteral dosage forms across a range of molecules from preclinical studies to commercialization.
  • The role involves providing strategic and technical leadership on program development teams, collaborating across functions, and supporting regulatory filings.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement, paid holidays, and vacation.

Matching Summary

Match Score: 85

Imsapharma Com Ar is seeking a Principal Scientist in Mixed Modalities for Sterile Product Development, responsible for the development of parenteral dosage forms. The ideal candidate will have significant experience in formulation science, leadership, and regulatory processes within a hybrid work environment.

Salary

$169,700.00 - $267,200.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision, retirement, paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • sterile product development
  • parenteral drug product development
  • formulation and process development
  • drug product composition
  • primary packaging selection
  • process scale-up and technology transfer

Nice-to-have

  • innovative thinking
  • professional collaboration
  • adaptability
  • leadership mentoring

Key Requirements

  • Ph.D. with 8+ years industry experience
  • M.S. with 10+ years industry experience
  • B.S. with 14+ years industry experience
  • experience with cGMP industrial background
  • experience with parenteral formulation and process development
  • experience with QbD principles
  • experience with process scale-up
  • experience authoring regulatory filings
  • demonstrated experience leading cross-functional teams

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter