Walk-in Interviews at Pune for Zydus Cadila

Zydus Cadila is one of Indias leading healthcare company and a global healthcare provider with strengths all along the pharmaceutical value chain. The groups state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centres are spread across Ahmedabad, Baroda and Mumbai (Thane).
We invite candidates for the following positions based at Ahmedabad for Commercial Vaccine Manufacturing and Zydus Biologics at Ahmedabad location. 
Viral Vaccine Production (Upstream Process):
Positions: Manager , Sr. Manager & DGM 
MSc. (Microbiology / Biotechnology / Biochemistry), B.Tech / M. Tech with Microbiology , Biotechnology / Biochemistry / Biosciences with 10 - 16 years of expertise in upstream operations . Candidates having experience in Influenza , Rabies, Measles, Mumps, Rubella and Varicella vaccine are most preferred. Should also have sound knowledge of the biological processes and GMP documentation. Must be familiar with cGMP requirements. 
Bacterial Vaccine Production (TOXOIDS ): 
Positions: Manager , Sr. Manager & DGM 
M.Sc. (Biotech / Microbiology) with 10-16 years of experience in the production of tetanus toxoid , Typhoid , diphtheria toxoid and conjugated vaccines at commercial scale are eligible . Should also be able to handle upstream fermentation processes and downstream TFF purification processes. 
Viral / Bacterial Vaccine Production ( fill finish formulation): 
Positions: Manager , Sr. Manager & DGM 
M. Pharm , MSc. (Microbiology, Biotechnology / B. Tech/ M. Tech with Biotechnology / Biochemistry with 10-16 years of experience in commercial Vaccine filling , packaging and dispatch are eligible . Must be familiar with cGMP requirements. Candidates having sound knowledge of lyophilization will be preferred.
Manufacturing Compliance & Technology Transfer : 
Positions: Sr. Executive , Manager, Sr. Manager & DGM 
M.Sc. (Biotech / Microbiology) with 4 16 in manufacturing compliance for handling QMS related issues (deviations, change controls, CAPA & investigations pertaining to manufacturing) and to ensure manufacturing as per established SOPs. Knowledge for preparation of regulatory dossiers for NRA, WHO Prequalification and GMP. Candidates having experience of Quality softwares ( Trackwise, LIMs, Lonza MODA etc.. ) and technology transfer mechanism are also invited for these positions.
For front liners
Viral Vaccine Production (Upstream Process):
MSc. (Microbiology / Biotechnology / Biochemistry), B.Tech / M. Tech with Microbiology/ Biotechnology / Biochemistry / Biosciences with 2 - 5 years of hands-on experience in upstream operations . Should also have sound knowledge of the biological processes and GMP documentation. Must be familiar with cGMP requirements. 
Seasonal Influenza / Rabies Vaccines : 
M.Sc. (Biotech/Microbiology) with 2-5 years of experience in Vaccine manufacturing. Should have experience in handling Embryonated egg based & Chick Fibroblast cell cultures. Experience in downstream process for virus purification, concentration by Zonal centrifuge / TFF will be preferred. 
Bacterial Vaccine Production (TOXOIDS): 
M.Sc. (Biotech / Microbiology) with 2-5 years of experience in the production of tetanus / diphtheria toxoids in a commercial plant. Should also be able to handle upstream fermentation processes and downstream TFF purification processes. 
Viral / Bacterial Vaccine Production ( fill finish formulation): 
M. Pharm , MSc. (Microbiology, Biotechnology ,B. Tech/ M. Tech with Biotechnology / Biochemistry with 2-5 years of hands-on experience on commercial purification of Vaccines ,filling , packaging and dispatch . Must be familiar with cGMP requirements. Candidates having sound knowledge of lyophilization will be preferred.
B.E./ B.Tech/Diploma (Mechanical, Electricals, Instrumentation): 
Must carry relevant experience in Manufacturing & Packing equipments, planning & execution for effective preventive & breakdown maintenance of process equipment like as Bio reactor, autoclaves, filling & packing lines, HVAC systems, utilities, QMS (CC/Deviations/CAPA), Energy monitoring, spare management. Operation & maintenance of HT & LT distribution , O&M of DG set, UPS, Transformers, power changeovers , PCC, MCC, DBs etc. Load list & SLD preparation, shall be familiar with ELV system design and execution and experience in i.e. BMS/ EMS/ FAS/ CCTV/ PA/ DI/ ACCESS/ PLC/ Scada/ HMI etc. Knowledge of electrical safety like as LOTO system, PPEs etc. Qualification etc. Calibration & validation of instruments / Equipments,. Independently handle fault analysis of PLC/SCADA/Instruments etc. D. Experience of injectable pharma plant & working in SAP system will be preferable. 
Production (Fill & Finish )
B.Pharma/ M. Pharm/ BE / ITI ( Mechanical/ instrumentation) with 2-10 Years of experience in formulation, filling, Packing & Visual activity. Should be able to handle PFS/Cartridges/Lyo vial/ Liquid Vial- filling line. . Knowledge of QMS - cGMP documentation/requirements. Must have sound knowledge on HMI / SCADA / PLC / mechanical trouble shooting/able to run automated/robotic arm high speed machine. Must be aware of Aseptic area operation. 

Quality Control (Protein analytics) (Bio assay) (Microbiology) (Physico chemical)
MSc. Biotechnology / Biochemistry/ Microbiology with 2-8 years of hands on experience of handling equipment such as HPLC/UPLC, CZE, UV Spectrophotometer, SDS-PAGE, IEF, RT-PCR, ELISA etc., should also have knowledge of handling stability studies and GMP documentation. Having experience in Bio Assay, experience of microbial identification, microbiological testing of material/products, sterility testing, BET, environmental monitoring of cleanroom, water system monitoring and microbiological validations/studies. Experience of handling equipment such as; HPLC, GC, IR, KF auto titrator, coulometer, melting points, should also have experience on chemical analysis of raw materials, water and packaging material. Knowledge in QMS and must be familiar with cGMP requirements. 
Quality Assurance: B. Pharm/M. Pharm- M.Sc.( Biotechnology/Biochemistry / Microbiology ) with 2-8 years of hands on experience of QA oversight activities, reviewing of batch manufacturing and QC analytical records, handling of qualification/validation, change control, deviation, investigation, CAPA, vendor qualification activities. Must be familiar with cGMP requirements. 

Details:

Date: 10th March, 2018

Time: 9.00 am to 5.00 pm

Venue: P4, Hinjawadi Rajiv Gandhi Infotech Park, Phase 1, Hinjewadi, Pune, 
Maharashtra 411057

Source : Naukri