Senior Scientist, Analytical R&D: Drug Analysis Innovator

MSD; Rahway (NJ); On-site; USD 117,000 - 184,000; Full time

Job summary

MSD in Rahway, NJ seeks a Senior Scientist to lead analytical development across early through late-phase programs, focusing on drug substances and dosage forms with GMP practices and regulatory submissions in mind.

You will drive method development, study design, and collaboration with internal and external partners, presenting findings at cross-functional forums and contributing to innovative analytical tools and data analysis capabilities.

Qualifications

• PhD or equivalent in chemistry or pharmaceutical sciences with relevant research track record.
• Experience designing and executing analytical studies for drug substances and products.
• Strong communication and leadership skills with regulatory exposure.

Responsibilities

• Drive analytical development solutions for small molecules, peptides, and oligonucleotides.
• Design studies to understand synthetic routes, formulations, and manufacturing processes.
• Implement analytical methods for development, release, and shelf-life under GMP.
• Provide leadership on drug development and analytical technology teams.
• Author regulatory submission documents and respond to agency questions.
• Document work clearly and timely; ensure collaboration with partners.
• Present results to project teams and cross-functional forums.
• Engage with external scientific communities and professional organizations.

Skills

Analytical Method Dev

Assay Development

Bioanalytical Analysis

Cell-Based Assays

Chromatography

NMR Analysis

UPLC

PAT

Technical Writing

GMP Environments

Strategic Thinking

Adaptability

Biochemical Assays

Large Molecule Characterization

Education

PhD in Chemistry/Pharma Sci

Master’s Degree in Chemistry/Pharma Sci + 3 yrs pharma exp

Bachelor's Degree in Chemistry + 7 yrs industry exp

Job description

MSD in Rahway, NJ seeks a Senior Scientist to lead analytical development across early through late-phase programs, focusing on drug substances and dosage forms with GMP practices and regulatory submissions in mind.

You will drive method development, study design, and collaboration with internal and external partners, presenting findings at cross-functional forums and contributing to innovative analytical tools and data analysis capabilities.