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.
To keep pace with our growth plans, we require young and skilled employees with experience in parenteral/injectable formulations for our manufacturing facility at Ahmedabad, Gujarat
Seeking a highly experienced Regulatory Affairs professional to manage regulatory activities for parenteral (injectable) products across the LATAM region.
Awareness on current Data Integrity requirements & cGMP requirements, Stability studies. Knowledgeable in handling OOS/OOT/Deviations and QMS (CAPA, CCP etc.) / LIMS Software.
Analysis of Raw material, Stability and Finished product samples, must have hands on experience of instruments like, HPLC, GC, UV, KF, ICPMS & IR etc., QC investigation and QMS.