Torrent Pharma is hiring for the position of Assistant Manager (Project Management-PDG) at its R&D Centre in Gandhinagar, Gujarat. This opportunity is suitable for pharma professionals with experience in OSD tablet and capsule project management and exposure to end-to-end pharmaceutical product development for the domestic market.
The role focuses on timely execution of product development projects from feasibility assessment to dossier submission. The selected candidate will coordinate with R&D, manufacturing, regulatory and commercial teams to help deliver compliant, cost-effective and market-ready formulations.
Job Details
| Company | Torrent Pharma |
| Position | Assistant Manager (Project Management-PDG) |
| Department | Product Development Group (PDG) |
| Job Location | R&D Centre – Gandhinagar, Gujarat |
| Qualification | B. Pharma / M. Pharma / MBA |
| Experience | 03 to 08 Years mandatory in Pharma OSD (Tablet/Capsule) Project Management |
Key Responsibilities
- 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 IFS with Purchase.
- Finalize CROs for bio-studies by 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 including Review 0-4 for API and formulation.
- Assess feasibility for product extensions into new markets.
- Maintain detailed understanding of the Product Development Roadmap with timelines across pre-formulation, formulation development, optimization and scale-up, analytical development, licensing and regulatory requirements, regulatory review, clinical and BA/BE study, commercial production and launch.
Site PDG Execution Responsibilities
- Plan and coordinate pilot, 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.
Required Qualifications
- B. Pharma, M. Pharma or MBA qualification.
- 03 to 08 years of mandatory experience in pharma OSD tablet/capsule project management.
- Experience in Product Development Group activities will be relevant for this role.
Required Knowledge and Skills
- Strong coordination skills across R&D, manufacturing, regulatory, commercial, purchase, QA/QC and plant teams.
- Understanding of pharmaceutical product development from feasibility assessment to dossier submission.
- Ability to monitor timelines, prepare MIS reports and support regulatory submissions.
- Working knowledge of OSD tablet/capsule development, scale-up, validation, stability, BA/BE and launch-related activities.
Why This Role Is a Good Opportunity
This role offers exposure to end-to-end pharma product development and project execution within the Product Development Group at Torrent Pharma’s R&D Centre in Gandhinagar. Candidates with OSD project management experience can work closely with cross-functional teams and contribute to timely development, regulatory readiness and commercial launch of formulations.
How to Apply
Interested candidates should share their updated profile on the email address below.
