MS&T - Technology Transfer (OSD)

Zydus Group; Ahmedabad District; On-site; INR 900,000 - 1,350,000; Full time

Job summary

Zydus Lifesciences seeks an Executive/Senior Executive for Technology Transfer at its Ahmedabad manufacturing facility. The role drives successful scale-up and transfer of solid oral dosage products from development to commercial manufacturing, ensuring compliance with quality and regulatory standards.

You will coordinate with Production, QA, Regulatory, Engineering, and Supply Chain, prepare MBRS and transfer docs, perform troubleshooting, and support process validation and site transfers to

Qualifications

• Hands-on experience in Technology Transfer, Scale-Up, Process Validation, or Manufacturing.
• Knowledge of solid oral dosage processes including tablets, capsules, granulation, compression, coating, and packaging.
• Experience with regulatory requirements, cGMP, and data integrity practices.

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 optimize batch sizes using scale-up principles and equipment capability assessments.
• Prepare, review, and update Master Batch Records (MBR), transfer documents, and validation protocols/reports.
• Coordinate with Production, QA, QC, Regulatory, Engineering, and Supply Chain for smooth transfer projects.
• Support process validation, revalidation, and site-to-site product transfers, and post-approval changes.
• Troubleshoot technical issues during scale-up and commercial manufacturing.
• Participate in process optimization, batch size modifications, and alternate vendor qualifications.
• Ensure compliance with cGMP, data integrity, regulatory requirements, and internal quality systems.
• Maintain project timelines and support product launches and regulatory submissions.

Skills

Technology Transfer

Scale-Up

Process Validation

Cross-functional Coordination

Education

B.Pharm

M.Pharm

Job description

• Designation : Executive / Senior Executive
• 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.