Company Jobs

Handling of Change Controls, CAPA's, Unplanned Deviations, Planned Deviation, Investigations and Audit Management in Trackwise software

To have knowledge of ICH guidelines and other regional regulatory requirements including USFDA, EMA, NMPA, TGA, CADIFA and other global regulatory market.

IPQA, Vendor Qualification, Technology Transfer, QMS, Validation, Qualification, Documentation Quality Risk Assessment

To develop promotional content and manage label updates in alignment with brand and regulatory requirements and ensure delivery of high-quality, compliant, and impactful content across multiple channels.

Actively leads product registrations by preparing / requesting documentation needed for complex filings. Employs project management skills to monitor activities and meet deadlines.

Identify, engage and onboard high-quality vaccinating clinics and specialist practices across Hyderabad and surrounding areas. - Build and maintain trusted relationships with dermatologists, consulting physicians, pulmonologists, rheumatologists, infectious disease specialists, transplant surgeons and other relevant clinicians. 

WALK IN DRIVE for M.Pharm, B.Pharm, M.Sc, B.Sc in Formulation Division

Handle QMS activitiesu su as OOS, OOT, Lab events. Support QC instrumentation, lab investigations, lab rounds.

AF90T/ AF150T/ ZRO 200/TTS/ Hartnett Printing / Band Sealing / ACG Capsule-Checkweighers/ Sensum / Tam Print/ Pressfit