Walk in Interview at Zydus Cadila in Quality Control, Quality Assurance, Packing
Zydus Cadila is one of India's leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharasahtra, Goa, Himachal Pradesh and Sikkim and the R&D Centers are spread across Ahmedabad, Baroda and Mumbai (Thane).
Post : Officer/ Executive/ Senior Executive/ Assistant Manager/ Deputy Manager
Quality Control (OSD) :
B.Sc. / B.Pharm / M.Sc / M.Pharm. with 2 to 8 years of hands-on experience of HPLC. GC, dissolution apparatus and UV-visible spectrometer. Should also have knowledge of weight analysis and stability studies for oral solid dosage forms.
Quality Assurance (OSD) :
B.Pharm / M.Sc / M.Pharm with 2 to 8 years of relevant experience in IPQA activities / environment monitoring in oral solid dosage / injectable manufacturing facilities. Packaging, manufacturing IPQA, warehouse IPQA, BPR review, batch release in SAP, calibration of IPQA instruments and having good knowledge of process validation, cleaning validation & packaging validation
Tablet / Capsule / Pellet / Wurster / Packing / Inspection
B.Sc / B.Pharm. / M.Pharm with 3 to 8 years of relevant experience in supervision operation, monitoring and related documents. Exposure of working in a regulatory plant is a must.
Technical Assistant - Tablet / Capsule / Pellet / Wurster / Packing / Inspection
Diploma Engineer with 3 to 8 years of relevant experience in operating machine. Vast experience in operating pharmaceutical machines in granulations - drying / coating / wurster / pellets / compression / blending, RMG, FBD, fette, MG2, sifting / blending area etc. Should have exposure to handling packing machines like capping machine, labeling machine, counter etc. Must have experience of handling inspection machines like sensum, viswill, enclony etc.
Deputy Manager/Associate Manager/Manager Investigator:
B.Pharm. / M.Pharm. with 7 to 10 years of relevant experience in IPQA activities / QMS / assessment of change controls / preparation and review of deviation / OOS / OOT investigation reports and market complaints investigations for oral solid dosage / injectable products. Candidates having a combination of QA and manufacturing experience will be preferred. The incumbent shall report to production and shall independently execute first hand investigations.
B.Pharm. / M.Sc. with 3 to 5 years of relevant experience in IPQA activities / QMS / assessment of change controls, system gap assessment (SOP v/s Practice), identification and implementation of corrective and preventive actions (CAPA) for the pharmaceuticals manufacturing facilities of oral solid dosage / injectable products. Candidates having add-on experience in manufacturing will have an added advantage.
Date : 15-16th October 2016
Location : Indore Timings : 09:00 AM 05:00 PM
Walk-In-Interview Venue : Fortune Park Galaxy. N.H. No. 8, G.I.D.C., Vapi - 396 195. Gujarat
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