Manager, QC at SANJIVANI PARENTERAL LTD. (2024-04 – Present)
Manufacturer of solid and liquid oral dosage forms
- Managing Quality Department, coordination with cross functional departments for smooth functioning
- Actively engaged in analytical method development and validation, cleaning method development and validation, cleaning process validation, process validation of new products
- Monitoring stability studies
- Preparation of SOPs and testing protocols of new products, Preparation of documents for regulatory submission
Dy. Manager, QC at WILLIAM ORGANIC (2021-10 – 2024-03)
Manufacturer of solid and liquid oral dosage forms
- Managing Quality Department to ensure quality management system is followed strictly, coordination with other departments for smooth functioning of manufacturing process
- Managing activities related to analytical method development and process validation for new products
Asst. Manager, Quality at UNIVET, Veterinary Medicines Ind. (L.L.C.) (2017-06 – 2021-07)
Veterinary Formulation unit catering for demand of local market in UAE, GCC countries, Iraq, Iran, Kenya, Ghanan etc.
- Looking after and managing activities related to quality of materials and products, including but not limited to sampling and analysis of raw materials, in-process and finished-products
- MLT of non-sterile RM/FP, AMV of FP & Cleaning methods
- Calibration of laboratory instruments
- Procurement of consumables
- Preparation of dossiers/MSDS for finished products
Sr. Executive, QC at HEMA LABORATORIES PVT. LTD. (2012-01 – 2017-06)
Contract manufacturer of Oral liquids and tablets (cephalosporin) for Abbott, Cadila Healthcare, Alembic Pharmaceuticals, Sun pharmaceutical, Blue Cross Laboratories, JB Chemicals, and Unichem Laboratories etc.
- Analysis and reporting of stability study samples and finished products
- Calibration of HPLC systems
- Execution of analytical method validation
- Review of bulk and finished product reports, log books, and methods of analysis
- Looking after for compliance of non-conformities observed during audits by contract manufacturer
Sr. Executive, QC at INTAS PHARMACEUTICALS (2008-11 – 2012-01)
Manufacturer of capsules, tablets, sustained release tablets, and inhalers. This manufacturing facility is catering to the demands of domestic as well as ROW markets.
- Writing of specifications, methods of analysis, and feeding in SAP system
- Preparation of working standards; procurement and inventory control of reference standards, chemicals/consumables, and instrument spares
- Review of process/method validation reports, and stability study reports
- Faced audits of ROW countries (Tanzania, Utopia, and Uganda)
Sr. Officer, QC at NECTAR LIFESCIENCES LIMITED UNIT VI (2007-01 – 2008-11)
Manufacturer of capsules, tablets, dry syrups and dry injections of cephalosporin group.
- Worked from project stage to full commercial production including carrying out water system validation, installation and calibration of laboratory instruments
- Preparation of working standards
- Procurement of reference standards, laboratory chemicals/consumables and spares
- Analysis and interpretations of results of active pharmaceutical ingredients
- Execution of cleaning validation and analytical method validation of finished products
