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Company Description Adcock Ingram Pharma Private Limited is a pharmaceutical company focused on delivering quality medicines and healthcare solutions. The organization emphasizes innovation, regulatory compliance, and patient safety across its products and operations. It offers opportunities for professionals to work in a structured, science-driven environment with established processes and standards. Team members collaborate across functions to support product development, manufacturing, and market access. The company values integrity, continuous improvement, and professional growth.
Role Description I am a Technology Transfer Officer with an M.Pharm in Pharmaceutics and experience in pharmaceutical manufacturing, technology transfer, process optimization, scale-up and GMP documentation.
My experience includes execution of technology transfer activities, process validation, packing validation and trial batches, along with preparation and review of MFR, BMR, BPR, SOPs and other GMP documents. I have also worked on deviations, change controls, CAPA, incidents, audit support and comparative dissolution profile (CDP) evaluations.
I collaborate with cross-functional teams including Production, Quality Assurance and Quality Control to support successful batch execution, process improvement and compliance with GMP requirements.
I am interested in developing my career in Regulatory Affairs, particularly in areas related to regulatory documentation, CTD/eCTD and global regulatory requirements.
Core strengths:
• Technology Transfer & Scale-Up
• Process Optimization & Validation
• GMP Documentation
• MFR / BMR / BPR
• SOP Preparation & Review
• Deviation, Change Control & CAPA
• Comparative Dissolution Profile (CDP)
• Pharmaceutical Equipment & Instrument Handling
• Audit Support
• Regulatory Affairs
Work arrangement
No
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