Principal Scientist, Intravitreal Product Development

Merck & Co., Inc.

Base: $173,200.00 - $272,600.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Ph.d. in pharmaceutical sciences or related field
6+ years industry experience in sterilization
Deep expertise in sterile drug product development
Merck & Co., Inc. is seeking a Principal Scientist for their Intravitreal Product Development team, focusing on sterilization science and sterility assurance in the development of sterile drug products. The role emphasizes technical leadership across various stages of product development and offers a hybrid work model

Job Summary

  • This role serves as a principal level sterilization scientist providing technical leadership for sterilization strategy and sterility assurance across injectable, ophthalmic, implantable, and inhaled dosage forms.
  • The successful candidate will influence development strategy, regulatory approaches, and manufacturing readiness while mentoring scientists and engineers in sterile product development and GMP compliance.
  • The position offers a competitive salary range of $173,200 to $272,600 along with comprehensive benefits including medical, dental, vision, and retirement plans.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Principal Scientist for their Intravitreal Product Development team, focusing on sterilization science and sterility assurance in the development of sterile drug products. The role emphasizes technical leadership across various stages of product development and offers a hybrid work model.

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, vacation

Skills & Requirements

Must-have

  • Ph.D. in Pharmaceutical Sciences or related field
  • 6+ years industry experience in sterilization
  • Deep expertise in sterile drug product development
  • Experience with terminal sterilization technologies
  • Knowledge of FDA and ICH regulatory expectations

Nice-to-have

  • Intravitreal product development experience
  • Experience with contract sterilization service providers
  • Knowledge of RTU container sterilization challenges
  • Track record of supporting global regulatory filings
  • Experience delivering technical training workshops

Key Requirements

  • Ph.D. with 6+ years experience or M.S. with 8+ years
  • Background in Chemical Engineering, Pharmaceutics, or Microbiology
  • Hands-on experience with sterilization cycle development and validation
  • Proven ability to lead cross-functional program teams
  • US work authorization required (Visa sponsorship available)

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter