July 2026

Exposure to OSD Manufacturing operations like Granulation, Compression, Coating, Pellet coating, Capsule filling, Primary Packing & Secondary Packing. Exposure of USFDA Plant.

Collaborate with peers across the organization to achieve client-centric delivery in a matrix organization. Collaboration across all stakeholders within Site Readiness

Person should know IPQA related activities of OSD Manufacturing activity.

Responsible for identifying and developing new business opportunities in Pharmaceutical Contract Manufacturing (CMO), Loan License Manufacturing (LLM), and R&D services for USA, CANADA, EU, UK and ROW Market.

Perform analysis of ointment, cream, gel, solution, raw material, and stability samples. Hands-on experience with HPLC, UPLC, GC, UV, IR, pH, viscosity, and assay testing.

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.

Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world.

Amgen is seeking a Senior Associate specializing in Commissioning & Qualification (C&Q) to join the Engineering C&Q Center of Excellence (CoE). In this role, you will support the preparation, coordination, and delivery of commissioning and qualification lifecycle documentation supporting engineering projects and GMP manufacturing systems across Amgen operations.

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