Analytical R&D Scientist (2nd Shift) — GMP Drug Analytics

Merck & Co.; Rahway (NJ); On-site; USD 90,000 - 120,000; Full time

Job summary

Merck & Co., Inc. in Rahway, NJ is seeking a Scientist to join a team of Analytical Chemists. The role focuses on GMP testing, method development, and data analysis to support small molecule, peptide, and oligonucleotide drug development in a dynamic, cross-functional setting.

The position operates on a 2nd shift (3:30 PM–11:30 PM) with emphasis on precise documentation, ALCOA-compliant records, and collaboration with Quality and Process Chemistry teams to drive robust analytical results.

Qualifications

• Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree.
• 1 year of relevant industry experience for applicants with a Master of Science degree in Chemistry, Pharmaceutical Sciences, or Life Sciences.

Responsibilities

• Support GMP testing activities for release and stability of APIs and formulations.
• Document experiments following ALCOA principles with clear, accurate records.
• Troubleshoot GMP testing issues with cross-functional teams and Quality.
• Validate analytical methods for release and stability of clinical materials.
• Prepare data entries, reviews, and analytical reports or summaries.
• Collaborate with Analytical R&D and Global Development Quality teams.

Skills

Adaptability

Analytical Chemistry

Analytical Development

Analytical Method Development

Analytical Reports

Chemistry

Data Entry

Data Review

GMP (GMP)

Laboratory Techniques

Multidisciplinary Teamwork

Self Motivation

Stability Testing

SOP Writing

Troubleshooting

Education

Bachelor of Science, Chemistry or Life Sciences

Master of Science in Chemistry or Pharmaceutical Sciences

Tools

Empower

LCMS

Data Science tools

Job description

Merck & Co., Inc. in Rahway, NJ is seeking a Scientist to join a team of Analytical Chemists. The role focuses on GMP testing, method development, and data analysis to support small molecule, peptide, and oligonucleotide drug development in a dynamic, cross-functional setting.

The position operates on a 2nd shift (3:30 PM–11:30 PM) with emphasis on precise documentation, ALCOA-compliant records, and collaboration with Quality and Process Chemistry teams to drive robust analytical results.