Analytical Chemist II – GMP/Pharma Lab

SUN PHARMA; New Brunswick (NJ); On-site; USD 69,000 - 77,000; Full time

Benefits offered by this job

Stable day-shift schedule

Annual bonus plan

Growth opportunities

Job summary

Sun Pharma in New Jersey seeks a detail-driven Chemist II to join our analytical laboratory team. You will perform testing of drug substances and products, ensuring quality, accuracy, and regulatory compliance in a cGMP environment.

The role involves hands-on work with HPLC/UPLC, GC, UV/Vis, FTIR, and dissolution equipment, along with data integrity, method development support, and timely reporting. Schedule is Monday–Friday, 8:30 AM–5:00 PM, with travel up to 10%.

Qualifications

• Bachelor’s degree in Chemistry or related field 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.
• Self-starter with hands-on, proactive, 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 (HPLC/UPLC, GC, UV/VIS, FTIR, particle size analyzer, Karl Fischer titrator).
• Ensure timely execution of testing and reporting of results.
• Maintain accurate documentation of raw data and test results.
• Assist with method development, transfer, and validation activities.

Skills

Analytical thinking

Verbal and written communication

Microsoft Office (Excel)

Problem solving

Education

Bachelor’s degree in Chemistry or related discipline

Master’s degree preferred

Tools

Excel

Job description

Sun Pharma in New Jersey seeks a detail-driven Chemist II to join our analytical laboratory team. You will perform testing of drug substances and products, ensuring quality, accuracy, and regulatory compliance in a cGMP environment.

The role involves hands-on work with HPLC/UPLC, GC, UV/Vis, FTIR, and dissolution equipment, along with data integrity, method development support, and timely reporting. Schedule is Monday–Friday, 8:30 AM–5:00 PM, with travel up to 10%.