Analytical QC Chemist II: HPLC/GC Expert in cGMP

Piramal Pharma Ltd; Lexington (KY); On-site; USD 60,000 - 90,000; Full time

Job summary

Piramal Pharma Solutions in Lexington, KY, is seeking a Chemist II for the Analytical Quality Control group. The role focuses on complex testing of raw materials, in-process and finished products, and instrument calibration to cGMP standards.

Reporting to the AQC Group Lead, you will apply HPLC/GC methods, document results per GDP, and mentor entry-level staff while ensuring accuracy and compliance in a fast-paced manufacturing environment.

Qualifications

• Bachelor of Science in Chemistry or related field.
• 5+ years QC lab experience with HPLC/GC.
• Experience with cGMP guidelines.
• Strong communication and documentation skills.
• Experience handling potent materials and parenteral products.

Responsibilities

• Perform routine/non-routine QC testing per SOPs and USP/EP/JP.
• Test raw materials, APIs, finished products, and stability samples.
• Operate and maintain HPLC/GC instruments.
• Document work per GDP and cGMP.
• Train entry-level QC personnel and act as SME.
• Write SOPs and reports; contribute to investigations.

Skills

HPLC analysis

GC analysis

cGMP compliance

Communication skills

Team collaboration

Education

Bachelor of Science in Chemistry

Tools

Microsoft Office

Laboratory instrumentation

Job description

Piramal Pharma Solutions in Lexington, KY, is seeking a Chemist II for the Analytical Quality Control group. The role focuses on complex testing of raw materials, in-process and finished products, and instrument calibration to cGMP standards.

Reporting to the AQC Group Lead, you will apply HPLC/GC methods, document results per GDP, and mentor entry-level staff while ensuring accuracy and compliance in a fast-paced manufacturing environment.