Senior Scientist, Analytical R&d

Merck & Co., Inc.

Rahway, NJ, USA
Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Late-stage method development and validation
Large molecule biologics and vaccines experience
Cgmp laboratory environment knowledge
Merck & Co., Inc. is seeking a Senior Scientist for their Analytical R&D team in Rahway, NJ, to lead the commercialization of large molecule products, including vaccines and biologics. The role involves overseeing analytical method development and validation while collaborating with both internal and external stakeholders to ensure successful product launches

Job Summary

  • This role is accountable for the commercialization of large molecule, vaccines, and biologics from Phase III through launch and transfer to supply.
  • The position involves directing and managing 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 with three days on-site per week and are eligible for an annual bonus, long-term incentives, and comprehensive benefits.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Senior Scientist for their Analytical R&D team in Rahway, NJ, to lead the commercialization of large molecule products, including vaccines and biologics. The role involves overseeing analytical method development and validation while collaborating with both internal and external stakeholders to ensure successful product launches.

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Annual bonus and long-term incentive eligible; 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
  • Assay life cycle activities oversight
  • ICH USP compendial chapter knowledge

Nice-to-have

  • Six Sigma and lean laboratory methodology
  • Global launch and supply experience
  • Regulatory filing support (BLA/MAA)
  • LIMS and software automation proficiency
  • Cross-functional stakeholder collaboration
  • Continuous improvement initiative leadership

Key Requirements

  • Bachelor's degree with 6 years industry experience
  • Master's degree with 4 years industry experience
  • PhD with 1 year industry experience
  • Minimum 2 years cGMP large molecule experience
  • US residency or citizenship required

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter