Zydus - Walk - In Interview on 28th Oct, 2018 Sunday at Hotel Fortune Park, Vallabha Road No-12, Banjara Hills , Hyderabad
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, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centers are spread across Ahmedabad, Baroda and Mumbai (Thane).
We invite candidates for the following positions based at Ahmedabad for our QC Function of Zydus Biologics (ZB) and Regulatory, Production and Engineering Functions of Vaccine Technology Centre based at Ahmedabad
Executive / Senior Executive
Quality Control – Bioassay
M.Sc/M.Pharm /B-Tech/M Tech with 2-5 years of hands on experience in executing of in-vitro cell based bioassays by Proliferation assays, Cytotoxicity assays, Apoptosis assay, Cytopathic assay, Receptor – ligand binding assay, Kinetic assays, Mycoplasma testing and Cell bank preparation, HCP/HCD methods
Quality Control – Validation
B-Tech/M Tech with 2-5 years of hands on experience in handling equipment & tests such as Validation of RP HPLC, Size exclusion chromatography, Ion exchange chromatography, Glycan Analysis of Biologics related complex molecules (Biosimilars and other Biologics molecules), Validation of Gel Electrophoresis/SDS PAGE Analysis methods, IEF Methods.
Quality Control – Protein
B-Tech/M Tech with 2-5 years of hands on experience in handling equipment & tests such as RP HPLC, Size exclusion chromatography, Ion exchange chromatography, Glycan Analysis of Biologics related complex molecules ( Biosimilar and other Biologics molecules), Gel Electrophoresis/SDS PAGE Analysis methods, IEF Methods.
Quality Control – RM & PM
M.Sc./B.Pharm / M.Pharm with 2-5 years of hands on experience in handling of equipment & tests such as Autotitrator, KF Titrator, U.V. Spectrophotmeter, FTIR & testing of Raw material.
Deputy Manager / Manager
Regulatory
M.Sc Biotechnology / Microbiology with 5-8 years of hands on experience in Filling Dossiers for National / International market, Submission of application for WHO prequalification, Submission of SLP’s of the batches for release. Keep up to date knowledge with national and international legislation and guidelines. Keep close track to regulatory changes and interpreting its implications on the drug development and authorization process. Collect, collate and evaluate scientific data from a range of sources. Prepare submissions of licence variations and renewals to strict deadlines. Develop timeline for responding to inquiries from regulatory agencies and ensures issues are addressed in a timely manner. Review company practices and provide advice on changes to systems
Manager & Sr. Manager
Viral Vaccine Production (Upstream Process):
M.Sc. (Microbiology / Biotechnology / Biochemistry)/ B.Tech / M. Tech with Microbiology, Biotechnology / Biochemistry / Biosciences with 10-16 years of experience in upstream operations. Candidates having experience in Influenza, Rabies, Measles, Mumps, Rubella and Varicella vaccine will be preferred. Should also have sound knowledge of the biological processes & GMP documentation. Fluency in English & Hindi speaking is mandatory.
Bacterial Vaccine Production (TOXOIDS)
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. Should be able to handle upstream fermentation processes and downstream TFF purification processes. Fluency in English & Hindi speaking is mandatory.
Viral / Bacterial Vaccine Production ( fill finish formulation):
M. Pharm/M.Sc. (Microbiology/Biotechnology) / B. Tech/ M. Tech with Biotechnology / Biochemistry with 10-16 years of experience in commercial vaccine filling, packaging and dispatch and familiar with cGMP requirements. Candidates having sound knowledge of lyophilization will be preferred. Fluency in English & Hindi speaking is mandatory.
Sr. Executive /Manager/Sr. Manager
Manufacturing Compliance & Technology Transfer:
M.Sc. (Biotech / Microbiology) with 4–16 years of experience in manufacturing compliance for handling QMS related issues (deviations, change controls, CAPA & investigations pertaining to manufacturing) and to ensure manufacturing as per established SOPs. Should have knowledge of 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. Fluency in English & Hindi speaking is mandatory.
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 and must be familiar with cGMP requirements. Fluency in English & Hindi speaking is mandatory.
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 and chick fibroblast cell cultures. Candidates with experience in downstream process for virus purification, concentration by zonal centrifuge / TFF shall be preferred. Fluency in English & Hindi speaking is mandatory.
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 be able to handle upstream fermentation processes and downstream TFF purification processes. Fluency in English & Hindi speaking is mandatory.
Viral / Bacterial Vaccine Production ( fill finish formulation) :
M. Pharm/ M.Sc. (Microbiology/Biotechnology)/B. Tech/ M. Tech with Biotechnology / Biochemistry with 2-5 years of hands-on experience in commercial purification of vaccines, filling, packaging and dispatch . Must be familiar with cGMP requirements. Candidates having sound knowledge of lyophilization will be preferred. Fluency in English & Hindi speaking is mandatory.
B.E./ B.Tech/Diploma (Mechanical, Electricals, Instrumentation) : Must have relevant experience in manufacturing & packing equipment’s, planning & execution of effective preventive & breakdown maintenance of process equipment like bio-reactor, autoclaves, filling & packing lines, HVAC systems, utilities, QMS (CC/Deviations/CAPA), energy monitoring and spare management. Should have exposure to operation & maintenance of HT & LT distribution, O&M of DG set, UPS, transformers, power changeovers, PCC, MCC, DBs etc., load list & SLD preparation. Should be familiar with ELV system design and execution and must have experience of handling BMS/ EMS/ FAS/ CCTV/ PA/ DI/ ACCESS/ PLC/ Scada/ HMI etc. Should have knowledge of electrical safety like LOTO system, PPEs, qualification, calibration and validation of instruments/equipments. Should be able to independently handle fault analysis of PLC/SCADA/Instruments etc. Candidated with experience of working in an injectable pharma plant and SAP system will be preferred. Fluency in English & Hindi speaking is mandatory.
Production (Fill & Finish)
B.Pharm/ M. Pharm/ BE / ITI (Mechanical/ instrumentation) with 2-10 years of experience in formulation, filling, packing and visual activity. Should be able to handle PFS/cartridges/lyo vial/ liquid vial filling line. Should have knowledge of QMS , cGMP documentation requirements, HMI / SCADA / PLC / mechanical trouble shooting and running automated/robotic arm high speed machine.
Must be aware of aseptic area operation. Fluency in English & Hindi speaking is mandatory.
Venue Details:
Day & Date: Sunday 28th Oct, 2018
Time: 9.00 am to 6.00 pm
Venue:
Hotel Fortune Park Vallabha
Road No-12, Banjara Hills, Hyderabad
