Roles and Responsibilities
- Online reveiew of batch production records.
- Review of in-process analysis report.
- Review of analytical documents.
- Online compliance to all cGMP, or any other regulatory requirements (Related SOPs)
- Handling of plant maintenance notification.
- Verification of in-process checks pf manufacturing process.
- Other QA activities on shop floor such as cleaning verification, validation activity.
QA activities would include documentation, validation, internal & external audit, master documentation creation, handling customer complaints and other department related activities. Exposure to DQ, IQ, OQ, PQ & regulatory audits like USFDA, MHRA, TGA is desirable
Time and Venue
Walkin Interview on 31st January from 9.30 AM – 4.30 PM onwards
MSN Laboratories Pvt Ltd Unit -I, Sy No: 317,320,321,322 , RudraramV,Patancheru M ,Sangareddy Dist, Telengana-502329