Instagram
youtube
Facebook

Exe/Sr Executive - Technology Transfer - Ms&T

2-8 years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: B.Pharm/M.Pharm Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Exe/Sr Executive - Technology Transfer - MS&T
Location: Multiple locations
Division: Corporate TS
Job Posted On: April 26, 2025
Employee Type: P-P8-Probationer-HO Executive


Job Overview

Zydus Life Sciences is seeking an experienced Executive/Sr. Executive for their Technology Transfer department in the MS&T (Manufacturing Science and Technology) division. The position is based at their Ahmedabad-based plant and requires candidates with a background in regulated pharmaceutical plants and experience in handling technology transfer processes.


Key Responsibilities

  1. Scale-up and Technology Transfer: Responsible for scale-up, technology transfer, and exhibit batches for commercial products.

  2. Site Transfer: Manage site transfer of approved products from one facility to another.

  3. Batch Size Selection: Evaluate and select optimal batch sizes for scaling up based on scientific techniques and manufacturing capacities for registration batches and commercial production.

  4. Documentation: Prepare and review master batch documents, validation protocols, and reports for submission batches and process validation.

  5. Cross-functional Coordination: Coordinate with Regulatory, Production, PPMC, QC, QA, and other functions for technology transfer activities.

  6. Revalidation and Troubleshooting: Handle revalidation, technical troubleshooting, batch size changes, and alternate vendor development.


Required Qualifications & Experience

  • Qualification: B.Pharma/M.Pharma

  • Experience: 2-8 years of experience in regulated plants with USFDA, MHRA, etc. approvals.

  • Skills: Hands-on experience in implementing cGMP and Good Documentation Practices.


Additional Details