MS&T - Technology Transfer (OSD)

Zydus Group

Ahmedabad District

On-site

INR 700,000 - 1,200,000

Full time

6 days ago
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Job summary

Zydus Lifesciences in Ahmedabad seeks an Executive/Senior Executive for Technology Transfer of solid oral dosage products from development to commercial manufacturing. The role requires coordinating cross-functional teams to ensure timely transfer and regulatory readiness.

Candidate should have 3–8 years of experience in pharma tech transfer, strong knowledge of cGMP and validation practices, and hands-on exposure to scale-up and documentation. This is an on-site role at our Ahmedabad facility.

Qualifications

  • Hands-on experience in Technology Transfer, Scale-Up, Process Validation, or Manufacturing of Oral Solid Dosage products.
  • Understanding of cGMP, regulatory requirements, and quality systems.
  • Strong documentation and data integrity skills.
  • Experience in site transfer activities and product launches is a plus.

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 per timelines.
  • Evaluate batch sizes using scale-up principles and equipment capability assessments.
  • Prepare and update Master Batch Records, technology transfer docs, and validation protocols.
  • Coordinate with Production, QA, QC, Regulatory Affairs, Engineering, and Supply Chain teams.
  • Support process validation, revalidation, site-to-site transfers, and change controls.
  • Troubleshoot technical issues during scale-up and manufacturing.
  • Participate in process optimization and continuous improvement initiatives.
  • Ensure compliance with cGMP, data integrity, and regulatory requirements.
  • Maintain project timelines and support product launches and regulatory submissions.

Skills

Tech Transfer
Scale-Up
Process Validation
Documentation
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.
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