Analytical Chemist II: Drug Testing & Method Validation

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

Job summary

SUN PHARMA is seeking a detail‑driven Chemist II to join the analytical laboratory team in New Jersey. You will perform routine analytical testing of materials and products, operate key instrumentation, and ensure data integrity in a cGMP environment.

The role emphasizes method development support, regulatory compliance, and accurate reporting. You will report results to supervisors and maintain clean, compliant laboratory records in a fast‑paced setting.

Qualifications

• Bachelor’s degree in Chemistry or related field; Master’s preferred.
• Minimum 4 years in a pharmaceutical analytical lab; or 3 years with a Master’s.
• Experience with wet chemistry and USP monographs.

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, dissolution, UV/Vis, FTIR, particle size analyzer, Karl Fischer titrator.
• Maintain accurate documentation of raw data, observations, and results.
• Assist method development, transfer, and validation activities.
• Ensure compliance with cGMP, ICH, FDA requirements and internal SOPs.
• Work Monday–Friday, 8:30 AM – 5:00 PM; travel up to 10%.

Skills

Excel

GMP/ICH/FDA knowledge

Analytical thinking

Communication skills

CEFR B1+ English

Education

Bachelor's degree in Chemistry or related field

Master’s degree preferred

Tools

HPLC

UPLC

GC

Dissolution apparatus

UV/Vis

FTIR

Karl Fischer titrator

Particle size analyzer

Job description

SUN PHARMA is seeking a detail‑driven Chemist II to join the analytical laboratory team in New Jersey. You will perform routine analytical testing of materials and products, operate key instrumentation, and ensure data integrity in a cGMP environment.

The role emphasizes method development support, regulatory compliance, and accurate reporting. You will report results to supervisors and maintain clean, compliant laboratory records in a fast‑paced setting.