Torrent Pharma Hiring Assistant Manager

Torrent Pharma, the flagship Company of Torrent Group is one of the leading pharma companies of the Country. The Company was a pioneer in initiating the concept of niche marketing in India and today is ranked amongst the leaders in therapeutic segment of cardiovascular (CV), central nervous system (CNS), gastro-intestinal (GI) and women healthcare (WHC).

Post : Assistant Manager (Project Management-PDG)

Department : Product Development Group (PDG)
Qualification : B.Pharma / M.Pharma / MBA
Experience : 03 to 08 Years. Mandatory in Pharma OSD (Tablet/Capsule) Project Management

JOB SUMMARY
This role drives end-to-end pharmaceutical product development for the domestic market, ensuring timely execution from feasibility assessment to dossier submission. It requires strong coordination across R&D, manufacturing, regulatory, and commercial teams to deliver compliant, cost-effective, and market-ready formulations.

KEY RESPONSIBILITIES
Product Development
• Conduct technical and commercial feasibility analysis for new product proposals.
• Define, monitor, and track project timelines using EPM/EPMS tools.
• Coordinate procurement of APIs, excipients, standards, and IFFs with Purchase.
• Finalize CROs for bio-studies considering cost, method availability, and criticality.
• Prepare and present monthly MIS reports with variance analysis to business heads.
• Lead regulatory submissions and promptly address queries.
• Conduct phase-wise project reviews (Review 0–4) for API and formulation.
• Assess feasibility for product extensions into new markets.
• Detail understanding of Product Development Roadmap with timeline – Pre-Formulation, Formulation Development, Optimization & Scale-up, Analytical Development, Licensing & Regulatory Requirements, Regulatory Review, Clinical & BA/BE Study, Commercial Production and Launching etc.

SITE PDG EXECUTION
• Plan and coordinate pilot bio, exhibit, and scale-up batches with PPC and plant teams.
• Ensure availability of plant documents and validation protocols.
• Oversee analytical validations, cleaning validations, and stability studies.
• Collaborate with QA/QC for timely testing, release, and dossier readiness.
• Address regulatory queries and ensure closure of deviations/OOS.
• Provide costing inputs for new launches and current year formulations.

Job Location : R&D Centre – Gandhinagar (Gujarat)