QA

RM Sampling and Analysis (Chemical & Instrumentation) HPLC, GC, IR, KF, UV, POLARIMETER, Dissolution Chemical Testing, FP/IP/Stability Analysis (Chemical & Instrumentation), Planning of AMT, AMV, API verification & Review

Experience in Packing Machines like Blister, BQS, Track & Trace, Hi cart Regulatory Experience is must, BMR & BPR Review, Documentation

IPQA ,ln process, Activities involve in shop floor activities .Review of Documents, QMS, Audit Exposer

QA documentation, SO Ps, CA PA, change control, and compliance. QC leadership, validation, OOS/OOT, audits, and compliance.

Method development & validation for tablets, capsules, creams & ointments. Exposure to US/EU regulatory requirements.

B.Sc./ M.Sc./ B.Pharm / M.Pharm. Manufacturing / Packing, Quality Control, Quality Assurance. Exposure to OSD Manufacturing operations like Granulation, Compression, Coating, Pellet coating, Capsule filling, Primary Packing and Secondary Packing. Working in USFDA Plant.

M.Sc/ B.Pharm / M.Pharm. To plan, prepare and review of high quality dossier with support and guidance, assuring technical concurrency and regulatory compliance, meeting agreed upon timeline.

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma; Experience Into Analytical Validation. Finished Goods. Raw Material. Stability & CLP

Handling of production machines such as BQS, Coating, Granulation. Bottle line packing machine primary and secondary.