Principal Scientist, Mixed Modalities, Sterile Product Development

Muckelab

Unknown
Base: $169,700.00 - $267,200.00; bonus/equity: eli...
Hybrid
Parenteral formulation and process development
Sterile product development expertise
Cross-functional team leadership
The Mixed Modalities team enables the translation of preclinical candidates into non-oral drug products by leveraging smart experimental design and cutting edge analytical tools

Job Summary

  • The Mixed Modalities team enables the translation of preclinical candidates into non-oral drug products by leveraging smart experimental design and cutting edge analytical tools.
  • The successful candidate will provide strategic and technical leadership on program development teams and mentor a small group of scientists.
  • We offer a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, and vacation.

Matching Summary

The Mixed Modalities team enables the translation of preclinical candidates into non-oral drug products by leveraging smart experimental design and cutting edge analytical tools.

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

Skills & Requirements

Must-have

  • Parenteral formulation and process development
  • Sterile product development expertise
  • Cross-functional team leadership
  • Quality by Design (QbD) application
  • Regulatory filings authoring
  • Process scale-up and technology transfer
  • Mentorship of junior scientists

Nice-to-have

  • Experience with intermediate modalities
  • Knowledge of sterile dosage forms
  • Alternate delivery technologies
  • Influencing regulatory strategies
  • Large capital project experience
  • Strong interpersonal and collaboration skills
  • Innovative thinking

Key Requirements

  • Ph.D. with 8+ years industry experience or equivalent
  • Experience with cGMP industrial background
  • Demonstrated scientific leadership and external publications/patents
  • Experience with FDA, ICH, and regulatory requirements for CMC
  • Ability to mentor junior scientists
  • U.S. work authorization required

Work Rights

US and Puerto Rico Residents Only

Sponsorship: available

Tailored Resume

Cover Letter