Principal Scientist, Mixed Modalities, Sterile Product Development

MOBS Lab

Rahway, New Jersey, USA
$169,700.00 - $267,200.00; bonus/equity: annual bo...
Hybrid
Parenteral drug product development
Sterile injectable 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 role requires providing strategic and technical leadership on program development teams, interfacing with key stakeholders, 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

$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, retirement benefits, paid holidays, vacation, and compassionate and sick days

Skills & Requirements

Must-have

  • parenteral drug product development
  • sterile injectable formulation
  • process development and scale-up
  • drug product composition
  • primary packaging compatibility
  • regulatory filings support
  • cross-functional team leadership

Nice-to-have

  • innovative thinking and problem solving
  • strong interpersonal collaboration skills
  • desire to learn and contribute
  • external academic community network
  • mentorship of junior scientists

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 QbD principles
  • experience authoring regulatory filings
  • working knowledge of FDA, ICH requirements

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter