33 Qc Documentation Jobs - Page 2

Role & responsibilities Inward/Outward Register QC Documentation like Inprocess/Finished Reports Stock Register maintaining Batch sheet maintain Courier Local and Export both Make COA for local parties Helping Vijaybhai to make any kind of documents like CAPA Making PO or any kind of documents if related department person is absent Making documents for ISO Audit Halal Documents Making supportive documents for party audit Maintaining Lab equipment calibration reports

Responsible for maintaining GDP and GLP in lab. Responsible for maintaining all laboratory testing documents according to GLP requirements and sustain all records in an accurate and legible manner Responsible for preparation of COA.

We are seeking a meticulous and experienced Manager Quality Control to lead and enhance our quality control operations at Synnat Pharma Private Limited. In this pivotal role, you will be instrumental in overseeing all aspects of quality control, ensuring adherence to Good Laboratory Practices (GLP), and maintaining a robust Quality Management System (QMS). Your expertise will be crucial in driving Analytical Method Development, managing CAPA and Change Control processes, and upholding Data Integrity standards. You will lead a team of QC analysts, providing training and mentorship to foster a culture of excellence. The ideal candidate will possess a strong understanding of ICH Guidelines and ...

Role & responsibilities Lead and manage the Quality Control team to ensure timely and accurate analysis of finished products (OSD & Injectables). Review and approve analytical reports, ensure compliance with GLP and cGMP standards. Oversee operations involving HPLC, GC, UV, IR , and other sophisticated instruments. Ensure proper implementation of MPCL and maintain all microbiological standards in compliance with regulatory guidelines. Handle all regulatory audits (USFDA, MHRA, WHO, etc.) and prepare necessary documentation. Manage OOS/OOT investigations and ensure CAPA implementation. Coordinate with cross-functional teams (QA, production, regulatory affairs) to ensure product quality. Train...

Good knowledge of QMS, Change control , Deviation. Having knowledge of Validation, APQR and other qulaity complience..Responsibilities: Perform analytical testing using various techniques, including HPLC, GC, UV-Vis, FTIR, and other relevant methods. Prepare and standardize solutions and reagents. Analyze and interpret test results, ensuring accuracy and compliance with specifications. Document all testing activities and results in accordance with GMP/GLP guidelines. Maintain and calibrate laboratory equipment. Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPA). Prepare and review QC documentation, including SOPs, test methods, and reports. ...

To get GA drawing approval from client in consultation with V TOP& Marketing Execute DQ. Documentation of project,tracking &reporting of project status report Update Brahma& reports, collect all reports like kick off Updating Drawing approval report Required Candidate profile Co-coordinating with factory & marketing team Co-ordination of activities between design, planning, material production and vendor management Keeping track of short supplies Updating PLC FDS

Role & responsibilities Develop, implement, and maintain Quality Management Systems (QMS) including AS9100 & ISO 9001 standards. Ensure inspection & testing of raw materials, subcontracted, in-process, and finished parts. Conduct and manage internal & external audits , ensuring compliance with industry standards. Investigate quality issues, perform root cause analysis , and implement corrective & preventive actions. Oversee calibration and maintenance of gauges, instruments, and test equipment . Manage supplier approvals/disapprovals and drive supplier quality improvement. Ensure compliance with ISO 14001:2015 EMS requirements. Guide, mentor, and train team members to maintain a customer-foc...

Develop QC formats for Inward Inspection, In-Process Inspection, Job-Work Inspection, and Finished Goods Inspection. Design and implement Operational Control Procedures (OCPs) for all key production stages. Monitor and verify QC reports generate