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.
Quality Assurance
Officer Dy. Manager (IPQA & QMS)
B.Pharm / M.Sc. / M.Pharm with 2 to 6 Years of relevant experience of IPQA and manufacturing QMS related activities in Oral Solid Dosage Manufacturing facilities.
Quality Control
Officer / Sr. Executive Quality Control (Analyst)
B.Sc./ B.Pharm / M.Sc. with 2 to 8 years of hands-on experience of analytical instruments like HPLC, GC, Dissolution apparatus and UV Visible Spectrometer. Should have experience of RM analysis, analytical Method transfer/Method validation and GLP.
Dy. Manager / Assoc. Manager Quality Control (Reviewer)
B.Sc./B. Pharm/ M.Sc. with 7 to 12 years of experience of Analytical data Review of Raw material & Method transfer/Method validation section.
Engineering
Technician Diploma/ITI with 3 to 8 years of experience in HVAC + BMS, HT, LT panels routine Operations, experience in Operations of Air Compressor, Chiller and Water system. Experience in OSD Process Equipment Maintenance. Experience in Instrument Sensors controls, Machine Operation, PLC, HML, SCADA, and experience in Calibration activity.
Senior Executive to Manager B.E / B.Tech (Mechanical/ Instrumentation/ Electrical/ Civil) with 4 to 15 years of experience in Scheduling and execution of preventive maintenance activities of OSD Process Equipment, HVAC + BMS Operations HT, LT panels, Installation and Upgradation. Scheduling and execution of preventive maintenance and In-house Calibration as well as external calibration activities. Maintenance of Air Compressor, Chiller and Water system. Knowledge of PLC,SCADA, HLM required.
Information Technology
IT CSV Engineer – Diploma. / B.E/ B.Tech/ MCA with 4 to 8 years of experience in IT department. Should have exposure of User Management (Q.C. /Manufacturing/ Engineering /Warehouse /Packing), GxP Systems, Desktop policy and CFR part 11 requirement. Preparation, Review and/or execution of validation documents and SOPs. Knowledge of Documentum, Trackwise and other quality software also required. Exposure to Pharma industry is mandatory.
Walk in Interview
Date : Sunday, 11th September 2022
Location : Vadodara
Timings : 9.30 a.m. – 5.00 p.m.
Venue : BARODA PRODUCTIVITY COUNCIL 2nd Floor, Productivity House, Productivity Road, Alkapuri, Vadodara 390007
See All B.Pharm Alerts M.Pharm Alerts M.Sc Alerts Ahmedabad Alerts
See All Other Jobs in our Database
.png)
