MS&T - Technology Transfer (OSD)

Company Name : Zydus Lifesciences Ltd Designation : Executive / Senior Executive Department: Technology Transfer (OSD - Solid Oral Dosage)Location: Ahmedabad PlantQualification: B.Pharm / M.PharmExperience: 3 to 8 YearsIndustry: Pharmaceuticals (Formulation Unit - Tablets, Capsules, Solid Orals)About the RoleZydus Lifesciences is seeking dynamic professionals for the Technology Transfer function at its Ahmedabad-based manufacturing facility. The role involves successful scale-up and transfer of pharmaceutical products from development to commercial manufacturing while ensuring compliance with quality, regulatory, and business requirements.Key ResponsibilitiesExecute technology transfer activities for solid oral dosage formulations from R&D to commercial manufacturing sites.Plan and coordinate exhibit, registration, validation, and commercial batches as per approved timelines.Evaluate and recommend optimum batch sizes using scientific scale-up principles and equipment capability assessments.Prepare, review, and update Master Batch Records (MBR), technology transfer documents, process validation protocols, and reports.Coordinate with Production, QA, QC, Regulatory Affairs, Engineering, and Supply Chain teams for smooth execution of transfer projects.Support process validation, revalidation, site-to-site product transfers, and post-approval changes.Perform technical troubleshooting during scale-up and commercial manufacturing activities.Participate in process optimization, batch size modifications, alternate vendor qualifications, and continuous improvement initiatives.Ensure compliance with cGMP, data integrity, regulatory requirements, and internal quality systems.Maintain project timelines and provide technical support for product launches and regulatory submissions.Desired Candidate ProfileHands-on experience in Technology Transfer, Scale-Up, Process Validation, or Manufacturing of Oral Solid Dosage products.Strong understanding of tablets, capsules, granulation, compression, coating, and packaging processes.Knowledge of cGMP, regulatory requirements, validation practices, and pharmaceutical manufacturing operations.Good analytical, documentation, and cross-functional coordination skills.Experience in commercial product launches and site transfer activities will be preferred.