Torrent Pharma is inviting applications for the position of Assistant Manager in Project Management within its Product Development Group (PDG) at the R&D Centre in Gandhinagar, Gujarat. The opportunity is suitable for pharmaceutical professionals with 3 to 8 years of experience in pharmaceutical oral solid dosage (OSD) project management. Candidates with B.Pharm, M.Pharm, or MBA qualifications and experience in product development, regulatory coordination, and pharmaceutical manufacturing are encouraged to apply. Interested candidates can share their updated profiles with the recruitment team at the email address provided below.<\/p>\n
Torrent Pharma Recruitment Details<\/h2>\n\n- Company Name:<\/strong> Torrent Pharmaceuticals Limited<\/li>\n
- Department:<\/strong> Product Development Group (PDG)<\/li>\n
- Position:<\/strong> Assistant Manager \u2013 Project Management (PDG)<\/li>\n
- Job Location:<\/strong> R&D Centre, Gandhinagar, Gujarat<\/li>\n
- Qualification:<\/strong> B.Pharm \/ M.Pharm \/ MBA<\/li>\n
- Experience:<\/strong> 3\u20138 years<\/li>\n
- Mandatory Experience:<\/strong> Pharmaceutical OSD (Tablet\/Capsule) project management<\/li>\n
- Application Email:<\/strong> [email\u00a0protected]<\/span><\/a><\/li>\n<\/ul>\n
Torrent Pharma Product Development Group Jobs<\/h2>\nAssistant Manager \u2013 Project Management (PDG)<\/h3>\n\n- Department:<\/strong> Product Development Group (PDG)<\/li>\n
- Qualification:<\/strong> B.Pharm \/ M.Pharm \/ MBA<\/li>\n
- Experience:<\/strong> 3\u20138 years<\/li>\n
- Mandatory Requirement:<\/strong> Experience in pharmaceutical oral solid dosage (OSD) project management.<\/li>\n<\/ul>\n
Job Summary<\/h4>\n
The role involves managing end-to-end pharmaceutical product development for the domestic market, ensuring timely execution from feasibility assessment to dossier submission. It requires coordination across R&D, manufacturing, regulatory, and commercial teams to deliver compliant, cost-effective, and market-ready formulations.<\/p>\n
Key Responsibilities \u2013 Product Development<\/h4>\n\n- Conduct technical and commercial feasibility analyses for new product proposals.<\/li>\n
- Define, monitor, and track project timelines using EPM\/EPMS tools.<\/li>\n
- Coordinate the procurement of APIs, excipients, standards, and IFFs with the Purchase department.<\/li>\n
- Finalize CROs for bio-studies, considering cost, method availability, and criticality.<\/li>\n
- Prepare and present monthly MIS reports with variance analysis to business heads.<\/li>\n
- Lead regulatory submissions and promptly address queries.<\/li>\n
- Conduct phase-wise project reviews, from Review 0 to Review 4, for API and formulation projects.<\/li>\n
- Assess the feasibility of product extensions into new markets.<\/li>\n
- Understand the product development roadmap and timelines, including pre-formulation, formulation development, optimization and scale-up, analytical development, licensing and regulatory requirements, regulatory review, clinical and BA\/BE studies, commercial production, and launch.<\/li>\n<\/ul>\n
Key Responsibilities \u2013 Site PDG Execution<\/h4>\n\n- Plan and coordinate pilot bio, exhibit, and scale-up batches with PPC and plant teams.<\/li>\n
- Ensure the availability of plant documents and validation protocols.<\/li>\n
- Oversee analytical validations, cleaning validations, and stability studies.<\/li>\n
- Collaborate with QA\/QC teams for timely testing, release, and dossier readiness.<\/li>\n
- Address regulatory queries and ensure the closure of deviations and out-of-specification (OOS) issues.<\/li>\n
- Provide costing inputs for new launches and current-year formulations.<\/li>\n<\/ul>\n
Eligibility & Qualifications<\/h2>\n
Candidates applying for the Assistant Manager \u2013 Project Management position should meet the educational and experience requirements specified in the recruitment advertisement.<\/p>\n
Eligible Educational Qualifications<\/h3>\n
B.Pharm | M.Pharm | MBA<\/p>\n
Experience Requirements<\/h3>\n\n- Required Experience:<\/strong> 3\u20138 years.<\/li>\n
- Mandatory Experience:<\/strong> Project management experience in pharmaceutical oral solid dosage (OSD) products, including tablets and capsules.<\/li>\n<\/ul>\n
Preferred Technical Skills<\/h3>\n\n- Pharmaceutical product development and project management.<\/li>\n
- Technical and commercial feasibility assessment.<\/li>\n
- Project planning and timeline tracking using EPM\/EPMS tools.<\/li>\n
- API and formulation development.<\/li>\n
- Regulatory submissions and dossier management.<\/li>\n
- Coordination with R&D, manufacturing, QA\/QC, regulatory, and commercial teams.<\/li>\n
- Validation, stability studies, and scale-up activities.<\/li>\n
- Cost analysis and monthly MIS reporting.<\/li>\n<\/ul>\n
Torrent Pharma Assistant Manager Job Location<\/h2>\n
The position is based at the Torrent Pharma R&D Centre in Gandhinagar, Gujarat.<\/p>\n
Job Location:<\/strong> R&D Centre, Gandhinagar, Gujarat, India.<\/p>\n![\"Torrent](\"https:\/\/pharmastuff.org\/wp-content\/uploads\/2026\/10\/Torrent-Pharma-Assistant-Manager-\u2013-Project-Management-1.webp\" "\\"Torrent")
<\/a>Torrent Pharma Assistant Manager \u2013 Project Management<\/figcaption><\/figure>\nHow to Apply<\/h2>\n
Interested and eligible candidates can share their updated profile or resume with the recruitment team using the email address below.<\/p>\n
Torrent Pharma Product Development Group Jobs<\/h2>\nAssistant Manager \u2013 Project Management (PDG)<\/h3>\n\n- Department:<\/strong> Product Development Group (PDG)<\/li>\n
- Qualification:<\/strong> B.Pharm \/ M.Pharm \/ MBA<\/li>\n
- Experience:<\/strong> 3\u20138 years<\/li>\n
- Mandatory Requirement:<\/strong> Experience in pharmaceutical oral solid dosage (OSD) project management.<\/li>\n<\/ul>\n
Job Summary<\/h4>\n
The role involves managing end-to-end pharmaceutical product development for the domestic market, ensuring timely execution from feasibility assessment to dossier submission. It requires coordination across R&D, manufacturing, regulatory, and commercial teams to deliver compliant, cost-effective, and market-ready formulations.<\/p>\n
Key Responsibilities \u2013 Product Development<\/h4>\n\n- Conduct technical and commercial feasibility analyses for new product proposals.<\/li>\n
- Define, monitor, and track project timelines using EPM\/EPMS tools.<\/li>\n
- Coordinate the procurement of APIs, excipients, standards, and IFFs with the Purchase department.<\/li>\n
- Finalize CROs for bio-studies, considering cost, method availability, and criticality.<\/li>\n
- Prepare and present monthly MIS reports with variance analysis to business heads.<\/li>\n
- Lead regulatory submissions and promptly address queries.<\/li>\n
- Conduct phase-wise project reviews, from Review 0 to Review 4, for API and formulation projects.<\/li>\n
- Assess the feasibility of product extensions into new markets.<\/li>\n
- Understand the product development roadmap and timelines, including pre-formulation, formulation development, optimization and scale-up, analytical development, licensing and regulatory requirements, regulatory review, clinical and BA\/BE studies, commercial production, and launch.<\/li>\n<\/ul>\n
Key Responsibilities \u2013 Site PDG Execution<\/h4>\n\n- Plan and coordinate pilot bio, exhibit, and scale-up batches with PPC and plant teams.<\/li>\n
- Ensure the availability of plant documents and validation protocols.<\/li>\n
- Oversee analytical validations, cleaning validations, and stability studies.<\/li>\n
- Collaborate with QA\/QC teams for timely testing, release, and dossier readiness.<\/li>\n
- Address regulatory queries and ensure the closure of deviations and out-of-specification (OOS) issues.<\/li>\n
- Provide costing inputs for new launches and current-year formulations.<\/li>\n<\/ul>\n
Eligibility & Qualifications<\/h2>\n
Candidates applying for the Assistant Manager \u2013 Project Management position should meet the educational and experience requirements specified in the recruitment advertisement.<\/p>\n
Eligible Educational Qualifications<\/h3>\n
B.Pharm | M.Pharm | MBA<\/p>\n
Experience Requirements<\/h3>\n\n- Required Experience:<\/strong> 3\u20138 years.<\/li>\n
- Mandatory Experience:<\/strong> Project management experience in pharmaceutical oral solid dosage (OSD) products, including tablets and capsules.<\/li>\n<\/ul>\n
Preferred Technical Skills<\/h3>\n\n- Pharmaceutical product development and project management.<\/li>\n
- Technical and commercial feasibility assessment.<\/li>\n
- Project planning and timeline tracking using EPM\/EPMS tools.<\/li>\n
- API and formulation development.<\/li>\n
- Regulatory submissions and dossier management.<\/li>\n
- Coordination with R&D, manufacturing, QA\/QC, regulatory, and commercial teams.<\/li>\n
- Validation, stability studies, and scale-up activities.<\/li>\n
- Cost analysis and monthly MIS reporting.<\/li>\n<\/ul>\n
Torrent Pharma Assistant Manager Job Location<\/h2>\n
The position is based at the Torrent Pharma R&D Centre in Gandhinagar, Gujarat.<\/p>\n
Job Location:<\/strong> R&D Centre, Gandhinagar, Gujarat, India.<\/p>\n<\/a>Torrent Pharma Assistant Manager \u2013 Project Management<\/figcaption><\/figure>\nHow to Apply<\/h2>\n
Interested and eligible candidates can share their updated profile or resume with the recruitment team using the email address below.<\/p>\n
- \n
- Department:<\/strong> Product Development Group (PDG)<\/li>\n
- Qualification:<\/strong> B.Pharm \/ M.Pharm \/ MBA<\/li>\n
- Experience:<\/strong> 3\u20138 years<\/li>\n
- Mandatory Requirement:<\/strong> Experience in pharmaceutical oral solid dosage (OSD) project management.<\/li>\n<\/ul>\n
Job Summary<\/h4>\n
The role involves managing end-to-end pharmaceutical product development for the domestic market, ensuring timely execution from feasibility assessment to dossier submission. It requires coordination across R&D, manufacturing, regulatory, and commercial teams to deliver compliant, cost-effective, and market-ready formulations.<\/p>\n
Key Responsibilities \u2013 Product Development<\/h4>\n
- \n
- Conduct technical and commercial feasibility analyses for new product proposals.<\/li>\n
- Define, monitor, and track project timelines using EPM\/EPMS tools.<\/li>\n
- Coordinate the procurement of APIs, excipients, standards, and IFFs with the Purchase department.<\/li>\n
- Finalize CROs for bio-studies, considering cost, method availability, and criticality.<\/li>\n
- Prepare and present monthly MIS reports with variance analysis to business heads.<\/li>\n
- Lead regulatory submissions and promptly address queries.<\/li>\n
- Conduct phase-wise project reviews, from Review 0 to Review 4, for API and formulation projects.<\/li>\n
- Assess the feasibility of product extensions into new markets.<\/li>\n
- Understand the product development roadmap and timelines, including pre-formulation, formulation development, optimization and scale-up, analytical development, licensing and regulatory requirements, regulatory review, clinical and BA\/BE studies, commercial production, and launch.<\/li>\n<\/ul>\n
Key Responsibilities \u2013 Site PDG Execution<\/h4>\n
- \n
- Plan and coordinate pilot bio, exhibit, and scale-up batches with PPC and plant teams.<\/li>\n
- Ensure the availability of plant documents and validation protocols.<\/li>\n
- Oversee analytical validations, cleaning validations, and stability studies.<\/li>\n
- Collaborate with QA\/QC teams for timely testing, release, and dossier readiness.<\/li>\n
- Address regulatory queries and ensure the closure of deviations and out-of-specification (OOS) issues.<\/li>\n
- Provide costing inputs for new launches and current-year formulations.<\/li>\n<\/ul>\n
Eligibility & Qualifications<\/h2>\n
Candidates applying for the Assistant Manager \u2013 Project Management position should meet the educational and experience requirements specified in the recruitment advertisement.<\/p>\n
Eligible Educational Qualifications<\/h3>\n
B.Pharm | M.Pharm | MBA<\/p>\n
Experience Requirements<\/h3>\n
- \n
- Required Experience:<\/strong> 3\u20138 years.<\/li>\n
- Mandatory Experience:<\/strong> Project management experience in pharmaceutical oral solid dosage (OSD) products, including tablets and capsules.<\/li>\n<\/ul>\n
Preferred Technical Skills<\/h3>\n
- \n
- Pharmaceutical product development and project management.<\/li>\n
- Technical and commercial feasibility assessment.<\/li>\n
- Project planning and timeline tracking using EPM\/EPMS tools.<\/li>\n
- API and formulation development.<\/li>\n
- Regulatory submissions and dossier management.<\/li>\n
- Coordination with R&D, manufacturing, QA\/QC, regulatory, and commercial teams.<\/li>\n
- Validation, stability studies, and scale-up activities.<\/li>\n
- Cost analysis and monthly MIS reporting.<\/li>\n<\/ul>\n
Torrent Pharma Assistant Manager Job Location<\/h2>\n
The position is based at the Torrent Pharma R&D Centre in Gandhinagar, Gujarat.<\/p>\n
Job Location:<\/strong> R&D Centre, Gandhinagar, Gujarat, India.<\/p>\n
<\/a>Torrent Pharma Assistant Manager \u2013 Project Management<\/figcaption><\/figure>\n How to Apply<\/h2>\n
Interested and eligible candidates can share their updated profile or resume with the recruitment team using the email address below.<\/p>\n
- Mandatory Experience:<\/strong> Project management experience in pharmaceutical oral solid dosage (OSD) products, including tablets and capsules.<\/li>\n<\/ul>\n
- Required Experience:<\/strong> 3\u20138 years.<\/li>\n
- Qualification:<\/strong> B.Pharm \/ M.Pharm \/ MBA<\/li>\n