Team Member -IPQA

Zoek Pin Indore, Madhya Pradesh


Permanent (Full time)

Recently Posted

Thoroughly check BMR, BPR, product labels and QC documents to ensure compliance before release of the batch / container. To ensure documents control as per SOP and timely submisstion documents as per 5S system. IPQA / cGMP round to be conducted in the all department to assurance cGMP compliance and verification of observation compliance within timeline. Perform the task delegated by the Management for any other roles and responsibilities either due to current or future business needs. Control sample and composite sample preparation as per SOP. Control sample verification as per schedule and report to supervisor if any abnormality observed during verification. Good to have To work with Production, R&D, QC and other department for the Investigation of Out of Specification (OOS), Deviation, Customer complaint and Internal audit observations. Online Annual Product Quality Review (APQR) preparation and review as per SOP and within defined timeline. Assist in implementing changes to processes, specifications, procedures, test methods, equipment and facilities.

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