5+

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.

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

Drive multiple medicinal and discovery chemistry projects with on-time, high-quality delivery. Serve as the primary scientific interface for global collaborators and provide strategic technical leadership.

Contribute to preparation and delivery of regulatory submissions from a global and regional perspective. Preparation and review of Marketing Authorization Applications & Variations for filing in US, EU, Japan, Canada Switzerland, Australia.