Senior Scientist, Analytical R&d

Merck & Co., Inc.

Rahway, NJ, USA
Base: $117,000.00 - $184,200.00; bonus/equity: ann...
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Late-stage method development and validation
Large molecule biologics and vaccines experience
Cgmp laboratory environment knowledge
** Merck & Co., Inc. is seeking a Senior Scientist in Analytical R&D for their Global Quality Large Molecule Analytical Sciences team in Rahway, NJ. This hybrid role focuses on method development, validation, and lifecycle management for large molecule products, including vaccines and biologics, and requires extensive collaboration with internal and external partners. **

Job Summary

  • This role is accountable for the commercialization of large molecule, vaccines, and biologics from Phase III through launch and supply transfer.
  • The position involves directing analytical activities within a global network of external manufacturing and testing sites to support on-time batch release.
  • Candidates will work in a hybrid model requiring three days on-site per week and are eligible for an annual bonus and comprehensive benefits package.

Matching Summary

Match Score: 75

** Merck & Co., Inc. is seeking a Senior Scientist in Analytical R&D for their Global Quality Large Molecule Analytical Sciences team in Rahway, NJ. This hybrid role focuses on method development, validation, and lifecycle management for large molecule products, including vaccines and biologics, and requires extensive collaboration with internal and external partners. **

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Annual bonus and long-term incentive available; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • Late-stage method development and validation
  • Large molecule biologics and vaccines experience
  • cGMP laboratory environment knowledge
  • Analytical technical transfer management
  • ICH USP compendial chapter expertise

Nice-to-have

  • Six Sigma and lean laboratory methodology
  • Experience with CMOs and contract testing labs
  • Regulatory filing support (BLA, IND)
  • Cross-functional stakeholder collaboration
  • Project timeline and deliverable management

Key Requirements

  • Bachelor's degree plus 6 years industry experience
  • Master's degree plus 4 years industry experience
  • PhD plus 1 year industry experience
  • Minimum 2 years cGMP experience in large molecules
  • US citizenship or work authorization required

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter