Posted:1 week ago|
Platform:
On-site
Full Time
Responsible for preparation of Revision of SOPs as per periodic review.
Responsible for preparation of New SOP as per requirement.
Responsible for preparation/revision of Site Master File (SMF), Validation Master Plan (VMP) & Quality Manual (QM).
Responsible for handling of Market Complaints regarding any product & Response CAPA with records.
Responsible for handling of Change Control as per requirement & maintain their Log book records accordingly.
Responsible for handling of Deviation regarding any Product/Process during operation and customer end and maintain their Log book records accordingly.
Responsible for review of Process Validation records, Qualification & Calibration records for any Product/Equipment as per requirement. (HVAC, Water System, Compressed Air & Production Machines)
Responsible for review/maintenance of Vendor Qualification records.
Responsible for Schedule Self-Inspection department wise and maintain the records accordingly.
Responsible for Preparation of Training Schedule & maintain the training records accordingly.
Any other task allotted by the senior.
Job Type: Full-time
Pay: ₹45,000.00 - ₹50,000.00 per month
Benefits:
Work Location: In person
Bioreva Sciences Limited
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Experience: Not specified
5.4 - 6.0 Lacs P.A.
Experience: Not specified
5.4 - 6.0 Lacs P.A.