Senior Scientist, Analytical R&d

Merck & Co., Inc.

Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid (3 days on-site, 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, specializing in the commercialization of large molecules, vaccines, and biologics. The role involves overseeing method development and validation while collaborating extensively with internal and external stakeholders to ensure successful commercialization and quality assurance

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 ensure on-time batch release.
  • Candidates will work in a fast-paced team focused on rapid advancement of the company's large molecule pipeline and growth of existing products.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Senior Scientist for their Analytical R&D team, specializing in the commercialization of large molecules, vaccines, and biologics. The role involves overseeing method development and validation while collaborating extensively with internal and external stakeholders to ensure successful commercialization and quality assurance.

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
  • 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 with 6 years industry experience
  • Master's degree with 4 years industry experience
  • PhD with 1 year industry experience
  • Minimum 2 years cGMP lab experience in large molecules
  • US residency or citizenship implied by location restrictions

Work Rights

Not specified

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