Evening Analytical Scientist – GMP & Data Analytics

Merck; New Jersey; On-site; USD 87,000 - 137,000; Full time

Job summary

Merck in Rahway, NJ seeks a Scientist in Analytical Chemistry to join a cross-functional team and enable development of small molecules, peptides, and oligonucleotides through laboratory analytics and data analysis. This second-shift role runs from 3:30 PM to 11:30 PM, with opportunities to impact API release, stability testing, and method validation.

You will document experiments, collaborate with Global Development Quality and Process Chemistry, and support audits while growing your career in

Qualifications

• Bachelor's degree with 3+ years of industry experience for BS holders.
• MS degree offers 1 year of relevant industry experience.
• Strong communication and teamwork skills are required.

Responsibilities

• Support GMP release and stability testing for APIs and formulations.
• Document experiments following ALCOA principles with accuracy.
• Troubleshoot GMP testing with cross-functional teams and QA.
• Validate analytical methods for release and stability of clinical materials.
• Perform data entry, review, and author reports or summaries.
• Collaborate with Analytical R&D and cross-functional partners.

Skills

Adaptability

Analytical Chemistry

Analytical Development

Analytical Method Development

Analytical Reports

ChemistryData Entry

Data Review

GMP

Laboratory Techniques

Multidisciplinary Teamwork

Self Motivation

Stability Testing

SOP Writing

Troubleshooting

Education

Bachelor's degree in Chemistry, Pharmaceutical Sciences, or Life Sciences

Master of Science in Chemistry, Pharmaceutical Sciences, or Life Sciences

Tools

Empower

LCMS

Job description

Merck in Rahway, NJ seeks a Scientist in Analytical Chemistry to join a cross-functional team and enable development of small molecules, peptides, and oligonucleotides through laboratory analytics and data analysis. This second-shift role runs from 3:30 PM to 11:30 PM, with opportunities to impact API release, stability testing, and method validation.

You will document experiments, collaborate with Global Development Quality and Process Chemistry, and support audits while growing your career in