Senior QC Scientist - Pharmaceutical Analysis & Testing

RXinsider LTD.; Piscataway Township (NJ); On-site; USD 85,000 - 105,000; Full time

Job summary

Amneal is seeking a Scientist 3 - QC to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, including products on stability, and to report results following SOPs and applicable cGMP guidelines.

You will participate in method transfer activities, assist with investigations, calibrate analytical instruments (HPLC, GC, UV, dissolution), and contribute to continuous improvement of analytical procedures and compliance.

Qualifications

• Bachelor's degree in Chemistry or related science; required
• Master's degree in Chemistry or related science; preferred
• 5+ years in BA/BS-level testing of chemicals/pharmaceutical products
• 3+ years in Master's level testing of chemicals/pharmaceutical products
• In-depth knowledge of analytical chemistry techniques (spectrophotometric, dissolution, chromatographic) and related instruments
• Ability to follow compendial procedures (USP/EP/BP/JP) and apply cGMP in QC lab

Responsibilities

• Perform physical and chemical analysis of raw materials, in-process and finished products per SOPs and specifications
• Participate in process validation and cleaning validation/verification testing
• Calibrate and operate HPLC, GC, and dissolution equipment; maintain instrument routine performance
• Document analyses, report results, and investigate data anomalies
• Review laboratory data for completeness and compliance with policies
• Assist with non-routine projects and instrument-related problem solving
• Provide hands-on training to Technicians or Scientists levels 1 and 2

Skills

Analytical chemistry

Data analysis

Troubleshooting

Instrument calibration

Education

Bachelor's degree in Chemistry or related science

Master's degree preferred

Tools

HPLC

GC

UV-Vis

Spectrophotometry

Dissolution testing

FTIR

Job description

Amneal is seeking a Scientist 3 - QC to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, including products on stability, and to report results following SOPs and applicable cGMP guidelines.

You will participate in method transfer activities, assist with investigations, calibrate analytical instruments (HPLC, GC, UV, dissolution), and contribute to continuous improvement of analytical procedures and compliance.