Analytical Chemist II — GMP, QC & Method Dev

Sun Pharmaceutical Industries, Inc.; New Brunswick, Northern (NJ, KY); Hybrid; USD 69,000 - 77,000; Full time

Job summary

Sun Pharmaceuticals seeks a detail‑driven Chemist II to join the analytical laboratory. You will test drug substances and products, ensuring quality and regulatory compliance in a cGMP environment.

The role emphasizes hands‑on lab work, instrument operation (HPLC/UPLC/GC, UV/VIS, FTIR), data integrity, and method development support. A Bachelor’s in Chemistry is required, Master’s preferred, with strong communication skills at CEFR B1+ level.

Qualifications

• Bachelor’s degree in Chemistry or related discipline required; Master’s preferred.
• Understanding of GMP, ICH, and FDA guidelines
• Proficiency in Microsoft Office, especially Excel
• Strong analytical thinking and problem‑solving skills
• Excellent verbal and written communication skills
• A self‑starter with a hands‑on, proactive, and team‑oriented approach
• English proficiency at CEFR Intermediate B1+ level

Responsibilities

• Perform routine analytical testing of raw materials, in‑process samples, blends, finished products, and stability samples.
• Operate and maintain analytical instrumentation, including HPLC/UPLC/GC, dissolution apparatus, UV/VIS, FTIR, particle size analyzer, and Karl Fischer titrator.
• Maintain concurrent and accurate documentation of raw data, observations, and test results.
• Assist with method development, method transfer, and method validation activities.
• Perform calibration and routine maintenance of laboratory instruments; ensure compliance with cGMP, ICH, FDA, and DEA requirements.

Skills

Analytical thinking

English proficiency (CEFR B1+)

MS Office / Excel

Education

Bachelor’s degree in Chemistry or related discipline

Master’s degree (preferred)

Tools

HPLC

UPLC

GC

Dissolution apparatus

UV/VIS

FTIR

Particle size analyzer

Karl Fischer titrator

Job description

Sun Pharmaceuticals seeks a detail‑driven Chemist II to join the analytical laboratory. You will test drug substances and products, ensuring quality and regulatory compliance in a cGMP environment.

The role emphasizes hands‑on lab work, instrument operation (HPLC/UPLC/GC, UV/VIS, FTIR), data integrity, and method development support. A Bachelor’s in Chemistry is required, Master’s preferred, with strong communication skills at CEFR B1+ level.