Principal Scientist, Intravitreal Product Development

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Base: $173,200.00 - $272,600.00; bonus/equity: ann...
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Sterilization cycle development and validation
Intravitreal product development experience
Contamination control strategies
** This job posting seeks a Principal Scientist in Intravitreal Product Development at a company focused on developing sterile drug products, including injections and implants, emphasizing sterilization science and sterility assurance. The ideal candidate should have extensive experience in sterile product development, regulatory knowledge, and strong leadership abilities while enjoying a hybrid work environment with comprehensive benefits. **

Job Summary

  • This role serves as a principal-level sterilization scientist providing technical leadership for sterile drug products including injectable, ophthalmic, and implantable dosage forms.
  • The successful candidate will define and implement sterilization strategies across all development stages while ensuring robust integration of formulation, packaging, and device compatibility.
  • Employees are eligible for an annual bonus, long-term incentives, and a comprehensive benefits package including medical, dental, vision, and retirement plans.

Matching Summary

Match Score: 75

** This job posting seeks a Principal Scientist in Intravitreal Product Development at a company focused on developing sterile drug products, including injections and implants, emphasizing sterilization science and sterility assurance. The ideal candidate should have extensive experience in sterile product development, regulatory knowledge, and strong leadership abilities while enjoying a hybrid work environment with comprehensive benefits. **

Salary

Base: $173,200.00 - $272,600.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays

Skills & Requirements

Must-have

  • Sterilization cycle development and validation
  • Intravitreal product development experience
  • Contamination control strategies
  • Regulatory submission support for CMC
  • Cross-functional technical leadership

Nice-to-have

  • Experience with contract sterilization providers
  • RTU container sterilization challenges
  • Facility design and qualification knowledge
  • Mentoring junior scientists
  • Global regulatory filing experience

Key Requirements

  • Ph.D. with 6+ years industry experience or equivalent
  • Deep expertise in sterile drug product development within cGMP
  • Proven experience with process scale-up and technology transfer

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter