Torrent Pharmaceuticals is inviting applications for the position of Assistant Manager – Project Management (Product Development Group) at its R&D Centre in Gandhinagar, Gujarat. This opportunity is intended for pharmaceutical professionals with experience in oral solid dosage (OSD) product development and project management involving tablets and capsules.
The role focuses on coordinating pharmaceutical development projects from initial feasibility assessment through formulation development, scale-up, regulatory submission and commercial launch. The selected candidate will work with cross-functional teams, including R&D, manufacturing, regulatory affairs, procurement, QA/QC and commercial functions, to support timely project execution.
Candidates with a B.Pharm, M.Pharm or MBA qualification and 3–8 years of relevant experience in pharmaceutical OSD project management can consider this opportunity.
Torrent Pharma Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Torrent Pharmaceuticals |
| Job Position | Assistant Manager – Project Management (PDG) |
| Department | Product Development Group (PDG) |
| Job Location | R&D Centre, Gandhinagar, Gujarat |
| Qualification | B.Pharm / M.Pharm / MBA |
| Experience | 3–8 Years |
| Required Domain | OSD Tablet and Capsule Project Management |
| Industry | Pharmaceutical |
| Application Mode | |
| Salary / CTC | Not specified |
About Torrent Pharmaceuticals
Torrent Pharmaceuticals is a pharmaceutical company involved in the development and commercialisation of pharmaceutical products. The current vacancy is associated with its Product Development Group at the R&D Centre in Gandhinagar.
The role supports the coordination of product development activities, helping align technical development, manufacturing readiness, regulatory documentation and commercial requirements.
Job Description
The Assistant Manager – Project Management (PDG) will coordinate pharmaceutical product development projects and monitor their progress against planned timelines and business requirements.
The position involves evaluating new product proposals, tracking development milestones, coordinating material procurement, supporting regulatory submissions and facilitating communication between internal departments and external service providers.
The selected candidate will also support site-level execution activities, including pilot batches, scale-up, analytical and cleaning validation, stability studies and preparation of product dossiers.
Educational Qualification
Candidates should have one of the following qualifications:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Master of Business Administration (MBA)
Experience Requirements
The vacancy specifies 3–8 years of experience in pharmaceutical OSD tablet or capsule project management.
Relevant experience includes:
- Pharmaceutical product development project coordination
- Tablet and capsule formulation development
- Project timeline management
- Scale-up and technology transfer activities
- Regulatory submission coordination
- Cross-functional project execution
- Manufacturing and launch readiness
Experience in Product Development Group activities is relevant to this position.
Key Responsibilities
1. Product Feasibility and Project Planning
- Conduct technical and commercial feasibility assessments for proposed products.
- Evaluate project requirements and identify important development milestones.
- Define and monitor project schedules using EPM/EPMS tools.
- Track progress against established timelines.
- Conduct phase-wise project reviews, including Review 0–4 for API and formulation projects.
- Assess opportunities for extending products into additional markets.
- Maintain an understanding of the product development roadmap.
2. Pharmaceutical Product Development Coordination
- Coordinate activities across pre-formulation, formulation development and optimisation.
- Track analytical development and scale-up milestones.
- Coordinate licensing and regulatory requirements.
- Monitor progress of clinical and bioavailability/bioequivalence (BA/BE) studies, where applicable.
- Support project progression towards commercial manufacturing and launch.
- Ensure relevant stakeholders understand project timelines and outstanding activities.
3. Procurement and External Vendor Coordination
- Coordinate procurement requirements for APIs, excipients, reference standards and IFS with the Purchase department.
- Support the selection of contract research organisations (CROs) for bio-studies.
- Evaluate CRO options based on cost, method availability and project criticality.
- Coordinate with internal teams and external service providers to support project execution.
4. Project Monitoring and MIS Reporting
- Maintain project trackers and monitor milestone completion.
- Prepare monthly Management Information System (MIS) reports.
- Present project progress and variance analysis to business heads.
- Identify delays, project risks and outstanding actions.
- Coordinate with relevant departments to support timely resolution of project issues.
5. Regulatory Submission and Documentation
- Coordinate regulatory submission activities for product development projects.
- Track dossier preparation and submission readiness.
- Support responses to regulatory queries.
- Coordinate with relevant teams to resolve documentation gaps.
- Monitor deviations and out-of-specification (OOS) issues and support their closure with the responsible functions.
Site-Level PDG Execution Responsibilities
Pilot, Exhibit and Scale-Up Batches
- Plan and coordinate pilot, exhibit and scale-up batches with Production Planning and Control (PPC) and plant teams.
- Track batch schedules and manufacturing readiness.
- Coordinate the availability of required plant documentation.
- Support preparation and availability of validation protocols.
Validation and Stability Activities
- Monitor analytical validation activities.
- Coordinate cleaning validation requirements.
- Track stability studies and related documentation.
- Work with QA/QC teams to support timely testing and release.
- Coordinate the availability of quality documentation needed for dossier preparation.
Costing and Commercial Launch Support
- Provide costing inputs for new product launches.
- Support costing activities for existing formulations in the current financial year.
- Coordinate with relevant functions to assess product development and commercialisation requirements.
- Help ensure technical, regulatory and manufacturing activities progress according to project plans.
Required Skills and Knowledge
Candidates should have knowledge or experience in the following areas:
- OSD tablet and capsule project management
- Pharmaceutical product development
- Technical and commercial feasibility assessment
- Project planning and timeline tracking
- EPM/EPMS tools
- Formulation development and optimisation
- Pilot and scale-up batch coordination
- Analytical and cleaning validation
- Stability studies
- BA/BE study coordination
- Regulatory submissions and dossier readiness
- MIS reporting and variance analysis
- API and excipient procurement coordination
- CRO coordination
- Cross-functional stakeholder management
- Manufacturing and commercial launch planning
Work Location
The position is based at the Torrent Pharma R&D Centre in Gandhinagar, Gujarat.
The role requires coordination with R&D, manufacturing, regulatory, commercial, Purchase, QA/QC and plant teams. It also involves project tracking, documentation and communication with external service providers where necessary.
Salary / CTC
The provided vacancy information does not disclose the salary or CTC for the Assistant Manager – Project Management (PDG) position. Candidates can request compensation details during the recruitment process.
How to Apply for Torrent Pharma Recruitment 2026
Interested and eligible candidates can share their updated profile through the recruitment email provided in the vacancy notice.
Email: rndhr@torrentpharma.com
Candidates should include their relevant pharmaceutical project management experience, educational qualifications and experience with OSD tablets or capsules in their profile.
Important Details Before Applying
- The position is Assistant Manager – Project Management (PDG).
- The department is Product Development Group.
- The job location is Gandhinagar, Gujarat.
- A B.Pharm, M.Pharm or MBA qualification is listed.
- The required experience is 3–8 years in pharmaceutical OSD tablet/capsule project management.
- The role involves end-to-end product development coordination.
- Knowledge of project tracking, regulatory documentation and manufacturing readiness is relevant.
- Applications are accepted through the listed recruitment email.
- Salary/CTC has not been disclosed.
Frequently Asked Questions
1. What position is Torrent Pharma hiring for?
Torrent Pharma is hiring for Assistant Manager – Project Management (PDG).
2. Where is the job located?
The position is based at the company’s R&D Centre in Gandhinagar, Gujarat.
3. What qualifications are accepted?
The vacancy lists B.Pharm, M.Pharm and MBA qualifications.
4. How much experience is required?
Candidates need 3–8 years of experience in pharmaceutical OSD tablet or capsule project management.
5. What does PDG stand for?
PDG stands for Product Development Group.
6. What are the main responsibilities?
The role covers project planning, product feasibility, development milestone tracking, procurement coordination, regulatory submissions, scale-up activities, validation, stability studies and commercial launch support.
7. Does the role involve regulatory work?
Yes. The responsibilities include coordinating regulatory submissions, preparing for dossier readiness and supporting the resolution of regulatory queries.
8. Is experience in tablet and capsule development relevant?
Yes. Pharmaceutical OSD tablet and capsule project management experience is specifically required.
9. Is salary mentioned?
No specific salary or CTC is provided in the vacancy notice.
10. How can candidates apply?
Candidates can send their updated profile to rndhr@torrentpharma.com.
Important Note
Vacancy availability, eligibility requirements and employment conditions may change. Candidates should verify the latest information with Torrent Pharmaceuticals before applying. This article is based on the provided recruitment details and is not an official recruitment notification issued by the company.