QC Chemist II — Instrumentation & Stability Testing

American Regent, Inc.; Shirley (MA); On-site; USD 79,000 - 85,000; Full time

Job summary

American Regent, Inc. is seeking a QC Chemist II to perform analytical testing on raw materials, in-process and finished product samples in the Quality Control Laboratories. The role emphasizes accurate identity, potency and purity testing in a regulated GMP setting.

You will operate instruments such as HPLC, GC, UV-Vis, AA and ICP, maintain GMP documentation, and ensure compliance with established procedures. Collaboration and independence are valued in this hands-on position.

Qualifications

• Bachelor’s degree in Science, Chemistry, Biology or related field required.
• Two years minimum pharmaceutical laboratory experience required.
• Knowledge of MS Word, Excel and Outlook.
• Adequate knowledge of Analytical Instruments such as HPLC, GC, AA, UV-VIS, ICP, etc.
• Detail oriented with strong time management skills and strong communication skills.
• Ability to work independently.

Responsibilities

• Operate instruments including HPLC, GC, AA, UV-VIS, ICP and other equipment.
• Perform testing of raw materials, in-process, and finished product samples.
• Perform all wet chemistry procedures including titrations and pH measurements.
• Maintain GMP documentation of all activities.
• Calibrate, troubleshoot and maintain laboratory instruments.
• Assist with general glassware cleaning and lab housekeeping.
• Perform other tasks as assigned by management.

Skills

Detail oriented

Time management

Communication skills

Independent worker

Education

Bachelor's degree in Science/Chemistry/Biology

Tools

HPLC

GC

AA

UV-VIS

ICP

MS Word

MS Excel

Outlook

Job description

American Regent, Inc. is seeking a QC Chemist II to perform analytical testing on raw materials, in-process and finished product samples in the Quality Control Laboratories. The role emphasizes accurate identity, potency and purity testing in a regulated GMP setting.

You will operate instruments such as HPLC, GC, UV-Vis, AA and ICP, maintain GMP documentation, and ensure compliance with established procedures. Collaboration and independence are valued in this hands-on position.