Mukund Bari

Direct and oversee analysis of in-process and finished product testing, and manage QMS activities including OOS, OOT, change control, CAPA, and incident investigation. Ensure GLP compliance and coordinate stability studies and regulatory audits.

Operated within central quality control laboratory supporting plant operations, overseeing work planning, sample allocation, and product release activities. Managed QMS activities and facilitated regulatory audits.

Directed analytical tasks across shifts in QC laboratory, conducted thorough analysis and testing of rifampicin products, and spearheaded coordination of QMS activities and audit readiness.

Ensured chamber stability via AMC/CMC coordination, calibration, validation, and execution of all chamber functions. Coordinated stability sample charging pull-out functions and leveraged LIMS for effective tracking.

Conducted stability sample and completed product analysis, performing analysis utilizing KF, UV, HPLC, and GC instruments. Sustained stability trend records and online laboratory documentation.

Received in-process samples for quality assurance and testing, conducted sampling of raw material solvents, and performed swab sampling to validate cleanliness. Conducted chemical analysis using Karl Fischer titration and executed testing using UV, HPLC, and GC instruments.

Received and distributed samples according to sections, performed material evaluation and testing, and crafted API finished product Certificate of Analysis (CoA). Preserved laboratory records in accordance with GLP guidelines.

Master of Science in Chemistry from Mumbai University, completed in 2016.