Qc Documentation Jobs – Apply to Latest Qc Documentation Job Vacancies

Analyst / Sr.Analyst - Quality Control Cadchem

1.0 - 4.0 years

2 - 3 Lacs

Punjab

Work from Office

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. Participate in internal and external audits. (Senior Analyst) Provide technical guidance and training to junior analysts. (Senior Analyst) Assist in method development and validation.

Posted 3 weeks ago

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QC Documentation Engineer Sai Placement

2 - 7 years

1 - 4 Lacs

Bharuch, Ankleshwar, Karjan

Work from Office

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

Posted 1 month ago

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Analyst / Sr.Analyst - Quality Control Cadchem Laboratories Ltd

1 - 4 years

2 - 3 Lacs

Punjab

Work from Office

Posted 2 months ago

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Lab-QA Titan Laboratories

5 - 7 years

5 - 6 Lacs

Mahad

Work from Office

Role & responsibilities Online monitoring of QC analysis along with respective raw data. Review of Analytical Test Reports for Raw Material, Packing Material, In-Process, Finished Product, Stability, and Working Standards. Review of analytical testing reports for validation, hold time study, cleaning validation, method validation, and method verification. Final review of Finished Product COA along with raw data. Review of Master Specifications for Raw Material, Packing Material, In-Process, Finished Product, Stability, MOA, Test Protocols, and Test Reports. Monitoring the withdrawal and analysis of stability samples as per the planner. Oversight of stability chamber-related activities. Monitoring the calibration of QC instruments as per the planner and SOPs, ensuring compliance and completion of calibration reports. Responsible for the review of QMS documents, including Change Control, Deviation, Incident, and Investigation. Initiation of Change Control, Deviation, Incident, and CAPA. Responsible for initiation of document Ratification and Errata. Investigation of OOS, OOT, and incidents in the QC laboratory. Review of metadata & Audit Trail in software as well as reports. Ensuring the maintenance of data integrity for documents and systems. Compliance with cGMP norms and regulatory requirements.

Posted 3 months ago

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