Pharma QC Chemist III — GMP Lab, On‑Site

Cipla; Town of Islip (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

Quality Control (QC) Chemist III at Cipla in Central Islip, NY on-site role. You will perform critical QC testing and data review to ensure GMP compliance and product integrity.

The position requires strong chromatographic skills (HPLC/UPLC/GC/IC), knowledge of GLP and GDP, and experience with Empower, LabSolutions, and LIMS/TrackWise. Collaboration with cross-functional teams and audits experience are valued.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field required.
• Master's degree preferred.
• Minimum 5 years of experience in pharmaceutical QC testing.
• Experience with chromatographic assays, impurity profiling, degradation studies, and stability evaluation.
• Knowledge of data integrity and computerized analytical systems compliance.

Responsibilities

• Perform raw materials, finished product, and stability testing in a GMP QC lab.
• Operate and troubleshoot HPLC, UPLC, GC, IC instruments.
• Ensure GLP, GDP, data integrity, and laboratory compliance.
• Maintain chromatography data systems and software (Empower, LabSolutions, Tiamo) and LIMS/TrackWise.
• Support and participate in audits (USFDA and customer audits).
• Collaborate with cross-functional teams and communicate results effectively.

Skills

HPLC

UPLC

GC

IC

Dissolution testing

FTIR

Education

Bachelor's degree in Chemistry or related field

Master's degree preferred

Tools

Empower

LabSolutions

Tiamo

LIMS

TrackWise

Karl Fischer

Job description

Quality Control (QC) Chemist III at Cipla in Central Islip, NY on-site role. You will perform critical QC testing and data review to ensure GMP compliance and product integrity.

The position requires strong chromatographic skills (HPLC/UPLC/GC/IC), knowledge of GLP and GDP, and experience with Empower, LabSolutions, and LIMS/TrackWise. Collaboration with cross-functional teams and audits experience are valued.