MS&T - Technology Transfer (OSD)

• Company Name : Zydus Lifesciences Ltd
• Designation : Executive / Senior Executive
• Department: Technology Transfer (OSD - Solid Oral Dosage)
• Location: Ahmedabad Plant
• Qualification: B.Pharm / M.Pharm
• Experience: 3 to 8 Years
• Industry: Pharmaceuticals (Formulation Unit - Tablets, Capsules, Solid Orals)

About the Role

Zydus 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 Responsibilities

• Execute 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 Profile

• Hands-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.