Role Summary: 

To perform routine and non-routine chemical analysis of raw materials, packaging materials, in-process samples, finished products, stability samples, and reference standards in accordance with approved specifications, pharmacopeial requirements, cGMP, GLP, and regulatory guidelines. The role ensures timely and accurate analytical support while maintaining data integrity, laboratory compliance, and continuous improvement of Quality Control operations.

Responsibilities: 

• Perform chemical analysis of raw materials, in-process materials, finished products, stability samples, and cleaning validation samples according to approved specifications and analytical methods.
• Execute analytical testing while ensuring compliance with cGMP, GLP, ALCOA+, Data Integrity, and Good Documentation Practices (GDP).
• Operate, calibrate, maintain, verify, and trouble...