Titan Biotech
Job description
What you’ll do
Roles and Responsibilities
Handling of ERP
Implementation of QMS
Directing all quality activities for the laboratory such as ILC, IQC, Training, etc.
To Perform and monitor document and data control of all controlled documents
To update all master documents periodically.
To prepare review of all SOPs, protocols and master controlled documents.
To do documentation related to OOS, Non conformity, Deviation, CAPA, Change
Control, Market Complaint Product recall.
To do audit compliance reports of internal/vendor/regulatory audits
To review new/revised artwork as per approved procedure.
To do preparation review of BPR, and all other documents as per QMS.
To maintain records of Vendor Development/ Qualification.
To prepare and review validation qualification documents.
Employment type
Full Time, Permanent
Education
B.Pharma in Any Specialization, B.Sc in Food Technology
About company
https://titanbiotechltd.com/
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