Senior Scientist, Analytical R&D — Advanced Drug Analysis

Merck; New Jersey; On-site; USD 110,000 - 160,000; Full time

Job summary

Merck in Rahway, NJ seeks a Senior Scientist to advance analytical methodologies for small molecules and related dosage forms. You will design and execute studies, implement GMP-compliant methods, and provide leadership across development programs.

Responsibilities include collaboration with internal and external partners, regulatory documentation, and presenting results in cross-functional forums. Travel is 5-10%.

Qualifications

• PhD or equivalent with strong publication record preferred.
• Experience with GMP environments and regulatory documentation.
• Proven ability to design and execute analytical development studies.

Responsibilities

• Drive solutions to analytical development challenges for small molecules, peptides, and oligonucleotide APIs and products.
• Design studies to understand synthetic routes, formulations, and manufacturing processes.
• Implement analytical methods for lab development as well as release and shelf-life assessment under GMP conditions.
• Lead innovation teams shaping future analytical methods and tools.

Skills

Adaptability

Analytical Method Development

Assay Development

Bioanalytical Analysis

Biochemical Assays

Cell-Based Assays

Chromatographic Techniques

GMP Environments

Innovative Thinking

NMR Analysis

PAT

Strategic Thinking

Technical Writing

UPLC

Education

PhD in Chemistry, Pharmaceutical Science, or related discipline

Master's Degree in Chemistry, Pharmaceutical Sciences, or related discipline plus at least 3 years of pharmaceutical industry experience

Bachelor's Degree in Chemistry, Pharmaceutical Sciences or related discipline plus at least 7 years of industry experience

Job description

Merck in Rahway, NJ seeks a Senior Scientist to advance analytical methodologies for small molecules and related dosage forms. You will design and execute studies, implement GMP-compliant methods, and provide leadership across development programs.

Responsibilities include collaboration with internal and external partners, regulatory documentation, and presenting results in cross-functional forums. Travel is 5-10%.