The QC Chemist / Analyst will be responsible for, but not limited to, the following duties:

Analytical Testing & Laboratory Operations

Perform routine and non-routine quality control analysis of raw materials, packaging materials, in-process samples, and finished pharmaceutical products in accordance with approved specifications and pharmacopeial methods.

Conduct HPLC analysis for assay determination, related substances testing, and impurity profiling of APIs and finished dosage forms.

Perform UV-Visible spectrophotometric, FTIR, and Karl Fischer, melting point analyses as required.

Carry out dissolution, comparative dissolution, and disintegration testing to support product equivalence and process optimization.

Ensure accurate analytical weighing and proper use of analytical balances.

Method Validation & Stability Studies

Reagents, Standards & Utilities

Equipment, Documentation & Compliance

Training & Team Support

• Perform routine and non-routine quality control analysis of raw materials, packaging materials, in-process samples, and finished pharmaceutical products in accordance with approved specifications and pharmacopeial methods.
• Conduct HPLC analysis for assay determination, related substances testing, and impurity profiling of APIs and finished dosage forms.
• Perform UV-Visible spectrophotometric, FTIR, and Karl Fischer, melting point analyses as required.
• Carry out dissolution, comparative dissolution, and disintegration testing to support product equivalence and process optimization.
• Ensure accurate analytical weighing and proper use of analytical balances.