Zydus Life Sciences is a renowned name in the pharmaceutical industry, committed to advancing healthcare solutions globally. Headquartered in Ahmedabad, India, the company specializes in creating innovative, high-quality, and affordable medications. With its state-of-the-art facilities accredited by USFDA, MHRA, and other regulatory agencies, Zydus consistently meets global standards in drug development and manufacturing.

Executive/Sr. Executive – Technology Transfer at Zydus Life Sciences

Job Role Overview

Zydus Life Sciences is seeking dynamic candidates for the role of Executive/Sr. Executive in Technology Transfer at its Ahmedabad-based plant. This role offers a unique opportunity for professionals with 2 to 8 years of experience in regulated environments to contribute to the company’s success.

Key Responsibilities

1. Scale-Up and Technology Transfer
   • Lead the scale-up and technology transfer processes for exhibit and commercial production batches.
   • Execute site transfers of approved products between facilities efficiently.
2. Batch Evaluation and Optimization
   • Assess and select optimal batch sizes using scientific scale-up techniques.
   • Ensure seamless production for registration and commercial launch batches.
3. Documentation and Validation
   • Prepare and review Master Batch Documents (MBDs), validation protocols, and reports.
   • Support submission batches and process validation activities.
4. Cross-Functional Coordination
   • Collaborate with Regulatory, Production, PPMC, QC, QA, and other departments to streamline technology transfer activities.
5. Technical Support
   • Address technical troubleshooting, manage batch size adjustments, and develop alternate vendor solutions.
   • Oversee revalidation processes to ensure compliance with cGMP practices.

Required Qualifications and Skills

• Education: Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm).
• Experience: 2-8 years of experience in regulated pharmaceutical plants with USFDA, MHRA, or similar approvals.
• Skills:
  • Proficiency in cGMP and Good Documentation Practices (GDP).
  • Hands-on expertise in technology transfer, scale-up, and validation activities.
  • Strong problem-solving and coordination abilities.
  • Excellent communication and teamwork skills.

Application Link