Bharathi Masi

Results-driven Pharmaceutical Production professional with over 4 years of hands-on experience in API (Active Pharmaceutical Ingredient) manufacturing across leading pharmaceutical organisations. Demonstrated expertise in operating GMP-compliant reactors, executing batch production of regulated drug substances, and supporting ISO and Indian Drug Safety Control regulatory audits. Holds an M.Sc. in Chemistry with a strong foundation in organic synthesis, reaction monitoring, and analytical testing.

Adept at adhering to cGMP, SOP documentation, and batch record review. Seeking a challenging role in pharmaceutical production, formulation and product excellence.

Production Operator | Pharmaceutical Manufacturing - Sthree Chemicals Private Limited

(2025-01)

• Perform in-process and finished-product quality control testing for Clemastine Fumarate API batches, ensuring compliance with pharmacopoeial specifications.
• Operate All-Glass Reactor (AGR) and Vacuum Tray Drier (VTD) with strict adherence to validated SOPs and GMP guidelines.
• Review and maintain batch manufacturing records (BMR) and batch packaging records (BPR), ensuring zero-defect documentation.
• Conduct sampling, wet-chemical analysis, and physicochemical tests; report deviations to senior QC management.
• Coordinate with production and regulatory teams to ensure timely release of batches meeting internal.

Production Operator | API Manufacturing - Orchid Pharma Limited

(2024-01 - 2025-01)

• Executed multi-step synthesis and downstream processing for Cefuroxime (Cemo) API in full compliance with cGMP standards.
• Operated industrial centrifuge equipment for product separation and isolation; performed regular equipment checks and maintenance logs.
• Participated in ISO and Indian Drug Safety Control regulatory audits; prepared relevant production documentation for audit readiness.
• Monitored critical process parameters (temperature, pH, pressure) and escalated out-of-specification events per established deviation procedures.
• Collaborated with QA/QC teams during in-process checks, contributing to an on-time batch completion rate.

Production Technician | API Manufacturing - Solara Active Pharma Sciences Limited

(2022-01 - 2024-01)

• Handled end-to-end production of Ibuprofen APIs using MGLR and GLR reactor systems under supervised GMP environment.
• Executed charge addition, reaction monitoring, workup procedures, and product transfer operations per validated batch records.
• Maintained detailed logbooks for reactor operations, raw material consumption, and in-process test results.
• Supported ISO and Indian Drug Safety Control compliance audits by preparing area documents, cleaning records, and equipment usage logs.
• Completed internal GMP and safety training modules; consistently followed PPE protocols and MSDS guidelines for hazardous reagents.

M.Sc.

• Chemistry - Bharathidasan University (2022-01 - 2024-01)

B.Sc.

• Chemistry - Govt Arts College, Chidambaram (Thiruvalluvar University) (2016-01 - 2019-01)

HSC (Class XII) - SKV Higher Sec School, Kurinjipadi (2014-01 - 2016-01)

SSLC (Class X) - SKV Higher Sec School, Kurinjipadi (2013-01 - 2014-01)