4-5

This role focuses on managing post-approval regulatory activities, including variations, renewals, and compliance with country-specific requirements. You will partner with cross-functional teams to ensure timely submissions and maintain regulatory dossiers.

The candidate should have hands-on experience in Change Control, Deviations, CAPA management, CAPA Closure, and overall QMS activities.

Injectable - Manufacturing (Aseptic (C-RAPS), Isolator, Ampule). Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

Compression, coating, granulation & blending. BMR and logbook maintenance for solid dosage forms. cGMP, SOP compliance, and QMS activities

Perform and review microbiological testing (EM, water, sterility, endotoxin). Ensure GMP and regulatory compliance (aseptic practices). Handle documentation, SOPs, and investigation

Finecure Pharmaceuticals Limited is a leading manufacturer and marketer of Pharmaceutical formulations in several therapeutic segments in dosage forms of Tablets, Capsules, & Dry Powders for Syrup having manufacturing locations at Sanand I Changodar Ahmedabad.

Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification. relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferred

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India