- Perform routine site inspections, identify quality non-compliances and conduct root-cause analysis to solve and prevent current and foreseen non-conformances- Perform raw materials and packaging tests and inspections per sampling plan to ensure they meet specifications and standards- Perform in-process and finished good inspections and tests like pH, viscosity, peroxide value measurement, melting point analysis and microbiological analysis per sampling plan to ensure product conforms to specifications and standards. - Perform line clearance and component verification, lot code verification, fill weights and seal integrity testing- Perform daily batch and production record review- Verify manufacturing equipment and site cleanliness- Check calibration and sanitation logs- Conduct sampling of products for stability, retention, and traceability- Conduct root cause analysis to investigate and address customer complaints- Assist with qualification, validation, and scale-up trials by identifying quality related challenges- Documentation of quality assurance activities, create audit reports, and propose recommendations for improvement- Create quality training materials and train plant personnel for compliance with good manufacturing practices (GMP)- All other functions and duties as may be assigned by immediate supervisor (R&D)- Perform QA activities with regards to GMP/GDP, SOPs, Deviation & Change control, NPN registration, Equipment Qualification, QMS management, Safety Standards, and plant policies & procedures.- Implementation of ERP software (Mar-Kov), prepared specifications for RM/PM.

- Involvement in the entire cycle of VTM product from bulk production to labelling of final product. - Strictly follow aseptic techniques to prevent the contamination of virus transport media (VTM).- Follow all standard operating procedure during production.- Perform daily inspection of final product i.e., labelling specification, content verification, properly capped tubes, appearance of media inside the tubes as per standard requirements.- Prepare final product and samples for QC inspection.- Provide labelling samples from printing machine for QA approvals.

- Prepare blister cards and package medications. - Operating and maintaining Synmed automated dispensing machinery.- Ensure number of pills in each package is correct.- Count each package quickly and accurately. - Ensure automated dispensing equipment has the correct and necessary supply of medication Clean and maintain automated dispensing equipment.- Maintaining inventory and ensuring proper stock levels.

- Performed regular analysis of raw materials and finished products and documented a manufacturing batch record accurately.- Maintained strict compliance with all safety regulations, accepted laboratory practices, SOPs and cGMP.- Managed the QC department daily activities such as in process quality control testing, lot release sample analysis.- Examined and released in-process materials to ensure packaging specifications are met and make sure all components are together as per standard requirements.