Walk in interview for M.Pharm, M.Sc, B.Pharm in QA, QC, Formulation at Ipca Laboratories
Ipca has been partnering healthcare globally in over 110 countries and in markets as diverse as Africa, Asia, Australia, Europe and the US. Ipca is a fully-integrated Indian pharmaceutical company manufacturing over 350 formulations and 80 APIs for various therapeutic segments. We are one of the world's largest manufacturers and suppliers of over a dozen APIs.
Sr. Officer/ Officer - Quality Control (Formulation) & Micro
Require Analyst/ Reviewer with experience of 2 to 10 years in Formulation products (i.e. Injection, OSD) analysis using for Wet lab/ Chemical / Stability & Micro lab with core exposure of instruments like HPLC7 GCV UV/ IR operations Micro related testing like Microbiology Lab, Bacterial Endotoxin Test (BET), Media Preparation. Validation protocol ,Validation of Sterility Test, Reconciliation & Water Analysis, Environmental Monitoring. Stability Sample Management, Protocol Preparation, QMS (OOS, OOT).
Qualification : 12th, B.Sc. / M.Sc. - Chemistry / Micro.
Injection/ Injectable - Formulation
Required Executive/ Officer with experience of 3 to 10 Years in Sterile area manufacturing (Ampoule and Vial), should have experience of Shift supervision, Knowledge of OOS, OOT, CAPA and handling of online documentation as per SOP/BMR. Well worse with instruments/equipments like Autoclave, Washing, Filling and sealing Machine etc. and concern activities related to batch manufacturing, filling, labeling, cartoning, 2D serialization, validation activities like media preparation, media filling.
Qualification - 12th, B.Sc / M.Sc./ B.Pharma/ M.Pharma
Engineering (Formulation - Maintenance)
Require engineer having 4 to 8 year experience of break down & trouble shooting at vial & ampoule line equipments of injectable facility, handling maintenance of machines like Vial washing. Vial Filling & sealine machine. Rotary washing. Filling & Sealine, inspection & Packing machines autoclave, Have exposure of trouble shooting of equipments knowledge of breakdown related to the tablet, liquid & injectable equipments.
Quality Assurance (formulation)
Required 3 to 6 yrs experience in IPQA (OSD), IPQA (Sterile), Qualification (Sterile, OSD), Validation (Sterile, OSD), regulatory affairs, OOS investigation (Microbiological), Risk Assessment, Market Complaint, QA Documentation, Exposure in QMS, Deviation, CAPA etc with Track wise system.
Qualification - B.Sc./M.Sc./ B.Pharma/ M.Pharma
Walk in Interview
Time & Date : 08th March 2020 on 10:30 AM to 05:00 PM
Address : PAPAYA TREE HOTELS.
Near Dr. Hardia Eye Clinic, AB Road, RAU - Indore (MP)
NOTE: Interested candidates, who are unable to attend walk-in interview can also E-mail: firstname.lastname@example.org. email@example.com. firstname.lastname@example.org
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