Preparation of documents for Compliance Report for Audit observations.
Review of documents for Compliance report for Audit Observations.
Follow up for supporting documents & activity for Compliance Report.
Arranging of all auditable files and supporting documents for Audit
Review of QMS documents
Preparation of supporting documents and Filling of Registration/Application forms
Preparation of Self inspection schedule and Follow up for Self-inspection Observation & Compliance Report
Updation of External audit details
Updation of THDC Certification details
Preparation & updation of organogram of Quality Assurance department
Responsible for release to intermediate stages during manufacturing.
Responsible for collection and submission of the analysis samples, control samples, stability samples and process validation samples or any other samples (as required).
Responsible for terminal inspection in FG.
Responsible for verification of production documents & log sheets (calibration, Area temperature etc.) in respective areas.
Responsible for review of completed batch record.
Responsible for Checking in-process activity in manufacturing, packing stages as per BMR & BPR instructions.
Responsible for periodic calibration of In-process instruments like , DT apparatus, weighing balance, pH meter etc.