Sr. Scientist, Analytical R&D

MSD • Rahway, NJ

3d • $117,000 - $184,200

About The Position

The Small Molecule Analytical Research and Development group is hiring a Senior Scientist based in Rahway, New Jersey. The role develops innovative analytical methodologies for early- through late-phase programs involving drug substances and a broad range of drug product dosage forms, combination products, and modalities. Work includes analytical characterization, imaging tools, and data analysis, and contributes to regulatory submissions supporting clinical trials. The role also provides scientific leadership on drug development projects and technology teams, collaborates with internal and external partners, and participates in the external scientific community. Travel is required, listed as 5–10% in the description and 10% in the posting details.

Requirements

• PhD in Chemistry, Pharmaceutical Science, or a related discipline; or a master’s degree in one of these fields plus at least 3 years of pharmaceutical industry experience; or a bachelor’s degree in one of these fields plus at least 7 years of industry experience.
• Proven record of strong technical problem-solving and innovative research experience, supported by scientific publications.
• Excellent written and oral communication skills.
• Strong leadership, collaboration, and interpersonal skills.

Nice To Haves

• Experience with large-molecule characterization, including oligonucleotides, enzymes, or peptides.
• Chromatography method development, analysis, and troubleshooting, such as LC or GC.
• Experience with advanced analytical techniques such as mass spectrometry or dissolution.
• Data science experience.

Responsibilities

• Develop solutions to analytical development challenges for synthetic small-molecule, peptide, and oligonucleotide active pharmaceutical ingredients and pharmaceutical products using conventional and novel technologies.
• Design scientific studies to inform selection and understanding of synthetic routes, formulation compositions, and manufacturing processes.
• Implement analytical methods for laboratory development and for release and shelf-life assessment of clinical supplies under GMP conditions.
• Provide leadership on drug development pipeline projects and innovative technology teams shaping future analytical methods and tools.
• Author regulatory submission documents throughout the project development lifecycle and respond to agency questions.
• Document work in a detailed and timely manner.
• Collaborate effectively with internal and external partners.
• Present experimental results and innovation efforts to project teams and cross-functional forums.
• Engage with the external scientific community through activities such as professional organizations, conferences, and publications.

Benefits

• Medical, dental, vision, healthcare, and other insurance benefits for employees and family.
• Retirement benefits, including 401(k).
• Paid holidays, vacation, compassionate days, and sick days.
• Eligible for an annual bonus and long-term incentive, if applicable.
• Domestic relocation.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree