Associate Principal Scientist, Small Molecule Analytical Research And Development

Merck Sharp & Dohme Corp

Rahway, New Jersey, United States
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (three days onsite, one day remote)
Phd in analytical chemistry or related field
3+ years pharmaceutical industry experience
Analytical control strategy development
Merck Sharp & Dohme Corp is seeking an Associate Principal Scientist for its Small Molecule Analytical Research and Development group in Rahway, NJ. The role involves developing innovative analytical methodologies for various drug types, collaborating with cross-functional teams, and contributing to regulatory submissions while fostering a culture of scientific excellence and mentorship

Job Summary

  • The role involves leading the development of innovative analytical methodologies for small molecules, peptides, mRNA, and bioconjugates from early stage through commercialization.
  • Candidates will be responsible for defining end-to-end analytical control strategies under GMP and authoring critical regulatory documents such as INDs, IMPDs, and NDAs.
  • The position offers a hybrid work model with three days on-site per week and includes eligibility for annual bonuses and comprehensive health benefits.

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking an Associate Principal Scientist for its Small Molecule Analytical Research and Development group in Rahway, NJ. The role involves developing innovative analytical methodologies for various drug types, collaborating with cross-functional teams, and contributing to regulatory submissions while fostering a culture of scientific excellence and mentorship.

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • PhD in Analytical Chemistry or related field
  • 3+ years pharmaceutical industry experience
  • Analytical control strategy development
  • Regulatory submission authoring (IND/NDA)
  • Method validation and specification setting

Nice-to-have

  • Hands-on chromatography method development
  • Mass spectrometry expertise
  • Mentoring junior scientists
  • High-throughput experimentation experience
  • External scientific publications

Key Requirements

  • PhD degree with 3 years experience OR Master's with 7 years OR Bachelor's with 10 years
  • Experience in pharmaceutical industry specifically
  • Strong written and oral communication skills
  • Ability to design and execute release and stability assays

Work Rights

Not specified

Tailored Resume

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