Should have experience to operating Blister Pack Machine ELMACH 3015 PDA and Auto Cartonator WKH100 and IMA PG IC1S0C) and Track & Trace Machine with Temper Evident.
The conference aims to promote understanding and implementation of GMP principles among pharmaceutical manufacturers, emphasizing the importance of adherence to GMP standards for the safety, efficacy, and quality of medicinal products. It will also provide guidance on incorporating GMP requirements into national medicines laws and regulations, and facilitate the exchange of best practices in GMP implementation. A Senior Official from Department of Pharmaceutical will be attending this Conference to address the delegates.
Water and Bioburden Testing and Microbiological limit testing, Sterility Testing and BET Testing, IQ,OQ and PQ of equipment, Trend Analysis preparation, Biological reactivity test, EM Observation - Moda exposure
B.Pharm, M.Sc, M.Pharm with 3-8 years of experience in IPQA and manufacturing, packing QMS related activities in oral solid dosage form tablets, capsules, soft gelatin capsules, pellet Dosage form manufacturing facilities.
Exposure of handling and compliance of various compression, coating and granulation machines, equipment Online documentation of BMR and log books during execution of batches.
Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management. Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times. Our legacy of over 70 years in healthcare and being dedicated to life in all its dimensions is reaffirmed in our new mission, vision and purpose. Unifying ourselves under the Zydus name, Cadila Healthcare Ltd., is renamed as Zydus Lifesciences Ltd.