Analytical Scientist I — Pharma QC & Method Development

Amneal Pharmaceuticals LLC; Piscataway Township (NJ); On-site; USD 65,000 - 80,000; Full time

Job summary

Amneal Pharmaceuticals LLC in New Jersey is seeking an entry-level Scientist-I who will support pharmaceutical analysis for drug product development, following schedules and SOPs to analyze drug substances, excipients, and drug product samples for release and stability.

The role uses USP/NF, EP methods and techniques like HPLC, GC, dissolution, spectrophotometry; ideal candidate has a BA/BS in Chemistry and at least one year in pharma, with knowledge of cGMP.

Qualifications

• Bachelor's Degree (BA/BS) in Chemistry or related science - Required
• 1 year or more in pharmaceutical experience
• Knowledge of US FDA- cGMP and SOP
• Understanding of analytical chemistry and analytical laboratory procedures
• Background of modern analytical laboratory techniques and use of HPLC, GC, TLC, UV, and analytical equipment
• Some knowledge of analytical Method development

Responsibilities

• Perform quantitative analysis for drug substances, excipients and products using USP/NF, EP, and in-house methods.
• Maintain compliance with US FDA cGMP regulations and internal SOPs.
• Analyze samples for release and stability testing.
• Interpret analytical results and communicate findings.
• Contribute to troubleshooting and optimize laboratory operations.

Skills

Spectrophotometry

HPLC

GC

Dissolution testing

Wet chemistry

Analytical problem solving

Communication of results

Education

Bachelor's Degree (BA/BS) Chemistry

Tools

HPLC

GC

TLC

UV

UV-Vis spectrophotometer

Job description

Amneal Pharmaceuticals LLC in New Jersey is seeking an entry-level Scientist-I who will support pharmaceutical analysis for drug product development, following schedules and SOPs to analyze drug substances, excipients, and drug product samples for release and stability.

The role uses USP/NF, EP methods and techniques like HPLC, GC, dissolution, spectrophotometry; ideal candidate has a BA/BS in Chemistry and at least one year in pharma, with knowledge of cGMP.