Assistant QC

Role & responsibilitiesComprehensive Oversight: Manage day-to-day activities in Quality Control .Instrument Expertise: Demonstrate hands-on experience with a variety of QC instruments, including HPLC, Dissolution, and other chemical and analytical tools.Lab Development: Utilize your expertise to develop the lab, ensuring compliance with the latest Revised...

Key Responsibilities:Manage all Analytical Quality Assurance (AQA) activities.Review, approve, and close Quality Management System documents related to QC.Act as Single Point of Contact (SPOC) for submission activities Dossier, Regulatory, Variation filings.Handle customer communications related to QA.Review manufacturing, packing, analytical reports of...

Manage QMS activities: Change Control, Deviation, CAPA, OOS, OOT, Lab Events.Conduct Risk Assessments, SOP reviews, and assist in grievance handling.Document & review: Specifications, SOPs, Test Data Sheets, Analytical Test Reports, and Master documents.Review Method Validation Protocols & Reports.Monitor calibration and preventive maintenance...

Analytical Testing: Assist the analytical testing processes for raw materials, in-process samples, and finished products.Quality Control Procedures: Implement robust quality control procedures in alignment with regulatory requirements and industry best practices.Instrumentation Management: To maintain laboratory equipment, ensuring calibration and validation...

Analytical Testing: Assist the analytical testing processes for raw materials, in-process samples, and finished products.Quality Control Procedures: Implement robust quality control procedures in alignment with regulatory requirements and industry best practices.Instrumentation Management: To maintain laboratory equipment, ensuring calibration and validation...

Following will be the responsibilities of the position holder:To ensure cGMP compliance at site.Responsible for Vendor Qualification and ManagementDay-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.To review vendor documents for Vendor Qualification.To perform the Vendor audit and its compliance...

Key Responsibilities1. Stability Study ManagementExecute stability studies as per guidelines and company protocols.Place, withdraw, and test samples from stability chambers (accelerated, intermediate, and long-term).Perform analysis of stability samples for physical, chemical, and microbiological parameters.Monitor and document environmental conditions of...

Following will be the responsibilities of the position holder:To ensure cGMP compliance at site.Responsible for Vendor Qualification and ManagementDay-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.To review vendor documents for Vendor Qualification.To perform the Vendor audit and its compliance...

Role & responsibilities1. Plant Operations and Management:Manage and monitor day-to-day operations of the solvent recovery plant, including distillation columns, reactors, condensers, and other associated equipment.Execute production schedules to ensure the timely recovery of solvents to meet the needs of the manufacturing plant.Perform start-up, shutdown,...

Key Responsibilities1. Stability Study ManagementExecute stability studies as per ICH guidelines (Q1A–Q1E) and company protocols.Place, withdraw, and test samples from stability chambers (accelerated, intermediate, and long-term).Perform analysis of stability samples for physical, chemical, and microbiological parameters.Monitor and document environmental...