QC Manager

Role OverviewWe are seeking a highly skilled and hands-on QC Manager to oversee quality functions across Incoming Quality Control (IQC), Process Quality Control (PQC), and Final Quality Control (FQC) for our SMT plant (two SMT lines). This role combines managerial responsibility with direct technical involvement in inspections, troubleshooting, and equipment...

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...

Role & responsibilitiesYou will be working as Head QC for USFDA approved Formulation Plant at Baddi and will be responsible for:You will be responsible for Establish the project goals and priorities.You will be responsible for team management and leadership.You will be handle 50 Plus Products and handle business turnover.You will be reporting to Head Quality...

Following will be the responsibilities of the position holder: 1. To ensure cGMP compliance at site. 2. Responsible for Vendor Qualification and Management 3. Day-to-day coordination with QA-representative w.r.t. Vendor Qualification/Re-Qualification and Management status.4. To review vendor documents for Vendor Qualification. 5. To perform the Vendor audit...

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...

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...

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...

Manage production activities in the Ointment & Liquid section per cGMP, SOPs, and safety guidelines.Supervise batch manufacturing and maintain accurate documentation. Coordinate with QA/QC, Engineering, and Stores for smooth operations