QA

Generate codes, issue control and un-control copies, and prepare master documents. Coordinate with F&D, ADL, and Quality Control for document management. Review SOP, Incident, Risk Assessment, Market Complain and Investigation.

Hiring for state-of-the-art formulation manufacturing facility - Granules Life Sciences, in Genome Valley, Shamirpet Hyderabad.

Manage bulk bottle, blister packing, Track and Trace, serialization and documentation. Handle machines like CVC, Servo, Countec, CAM, BQS, HONGA and UHLMANN.

BPharm or MPharm require; Review of Protocols and reports related to Analytical method validation, Verification of API and Finished product, Vendor qualification, cleaning validations. Hypothesis analysis, general validations, Stability, photo stability, thermal cycling, in use, split study and miscellaneous studies and approval in LIAAS where ever applicable.

Torrent Pharma has a broad portfolio, comprising BGx medicines, which keeps us ahead in bringing quality medicines for patients all over the globe.

Review of technology transfer documents and initiate the validation accordingly in plant scale by coordinating with CFT. Review of Master Batch Manufacturing records executed Batch manufacturing records.

Competent in Analytical methods validations and transfers of Drug substances and Drug Products. Experience in drafting investigation reports and protocols

Review of specification, Method of analysis Protocol, heanding of OOS and OOT, Investigation and lab event, review and approval of QC documents.