Ipca Laboratories Limited Walk-in Interview .Ipca Laboratories Limited Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Important Details :
Ipca Laboratories Limited Openings
Job Description –
Require experience and exposure of powder processing area,Batch Planning, Manpower Handling, Production, Batch Manufacturing, Reactors, GMP, Filters, Centrifugation, GLR, Dryer, Centrifuge, Filtration, SSR, FBD, RCVD, VTD, STD, JET MILL, MULTI MILL, BLENDER, SHIFTER ETC.Performing unit operations as per respective BPR. To ensure cleanliness of process equipment and plant. To verify Quantity of Raw materials and Intermediates are as per BPR.
Job Description –
Require engineering experience of mechanical & Electrical break down & trouble shooting, routine repairs and maintenance activities (Plant Maintenance) of all API equipments like Reactors, Filters, Centrifugation, GLR, Dryer, Centrifuge, SSR, FBD, RCVD, VTD, STD, JET MILL, MULTI MILL, BLENDER, SHIFTER ETC. Also in Engineering Pharma Projects- Civil/Mechanical, Documentation knowledge like DQ, IQ, OQ. Audit faced USFDA & other audits preferred.
Job Description –
Require Analyst/ Reviewer with experience of API products analysis using for Wet lab/ Chemical / Stability / Inprocess Lab & Micro lab instruments like UV, Autotitrator, Muffer Furnance, IR, Potentiometer, Karlfisher, pH meter etc. analytical exposure in HPLC/ GC/ LCMS/ GCMS operations & Micro related testing like Microbiology Lab,Validation protocol ,Validation of Sterility Test MLT, Microbiological limit Test Reconciliation & Water Analysis,Temperature & Environmental Monitoring. Also expertise in Stability Sample Management, Protocol Preparation.
Trouble Shooting experiments.
To assist production 1QA 1QC 1 EHS team for the OOS lOOT 1deviation 1 market , complaints and major incidents investigation by providing technical inputs and necessary experimentation.
To inVolve in scale up of the developed technologies from lab scale to pilot and commercial scale. .
To involve in transferring of analytical method to IPQC 1 QC.
Responsible for preparation, review and maintenance of all the necessary records, documentation, SOP compliance and the training for PCE Lab.
Candidates who will attend the walk in Interview, please keep the below mentioned documents* :
Updated Resume, Passport size photograph, Educational Testimonials, Experience Certificates, Salary slips (last 3 months) with salary structure*.
Email Id : Shivani.verma@ipca.com & jyotik.yadav@ipca.com, Yogesh.panchal@ipca.com
Formulation
Job Description –
Required of experience in Sterile area manufacturing (Ampoule and Vial) Shift supervision, Knowledge of OOS, OOT, CAPA, online documentation as per SOP/BMR. 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 & Packing.
Quality Assurance
Designation – Officer / Executive .
Experience – 4 to 10 Years.
Qualification – B.Sc / M.Sc / B Pharma / M. Pharma .
Job Description –
Require experience in IPQA, IPQA (Sterile), Qualification (Sterile,), Validation (Sterile), Analytical QA, Stability Studies, regulatory affairs, OOS investigation (Microbiological), Risk Assessment, Market Complaint, QA Documentation, Exposure in QMS, Deviation, CAPA etc with Trackwise system.
Candidates who will attend the walk in Interview, please keep the below mentioned documents* :
Updated Resume, Passport size photograph, Educational Testimonials, Experience Certificates, Salary slips (last 3 months) with salary structure*.
Email Id : Shivani.verma@ipca.com & jyotik.yadav@ipca.com, Yogesh.panchal@ipca.com
Time and Venue
16th November , 10.00 AM – 5.00 PM
Venue – Ipca Laboratories Ltd, Pologround, Indore (M.P) Date – 16th November 2025, Time – 10:00 to 17:00
Contact – Jyoti Yadav , Shivani Verma
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