Skip to main content

Zydus Cadila: Walk-in Interview on 9th April 2017

Zydus Cadila

Logo


PUNE
 Walk in interview on 9th April 2017

An opportunity for you to join our manufacturing plant at Ahmedabad

*Officer / Executive / Senior Executive / Assistant Manager / Deputy Manager / Manager*

*Vaccine Manufacturing*
M.Sc. (Microbiology / Biotech) with 1 to 12years of hands-on experience in candling of specific pathogen-free eggs (SPF), embryo isolation, complete MEM preparation, initiation of primary cell culture, cell count, sampling of material for sterility testing during production process, scale up of production processes for cell culture based rabies vaccine and egg-based trivalent & tetravalent influenza vaccines.

*Viral Vaccine Production* (Upstream Process):
M.Sc. (Microbiology/Biotechnology / Biochemistry) / M.Tech / B.Tech with Biotechnology /Biochemistry / Biochemical Engineering with 1 to 12 years of hands-on experience in upstream operations like handling cell lines, cell culture, tissue culture, cell culture media preparation, sterilization by membrane filtration and cell line / ELISA based in-process quality tests. Candidates having exposure to handling of MRC5 cells, Vero cells for manufacturing measles, mumps, rubella and varicella vaccine are preferred.

*Viral Vaccine Production* (Downstream Process / Fill Finish Formulation):
M.Pharm / M.Sc. (Biotechnology) / B.Tech / M.Tech with Biotechnology / Biochemistry / Biochemical Engineering with 3 to 8 years of hands-on experience in commercial purification of recombinant proteins, filling, Lyophilization, packaging and dispatch. Should also have sound knowledge of downstream operations / buffer preparation / solubilisation/ refolding / chromatography and GMP documentation.

*Quality Control - (Analyst category)*:
B.Sc. / B.Pharm / M.Sc. with 2 to 8 years hands-on experience of HPLC, GC, dissolution apparatus and
UV-visible spectrometer. Should also have knowledge of wet analysis, stability studies, for parenteral preparations and solid dosage forms.

For all the positions, candidates should also have sound knowledge of the biological processes and cGMP documentation and must be familiar with cGMP requirements. Fluency in speaking Hindi and English is mandatory. Interested candidates may “Walk-in” for an interview along-with their updated CVs, Salary Slip and relevant documents as per below schedule:

Walk-in-interview
Date: Sunday, 9th April, 2017
Timings: 9.30 a.m. - 5.00 p.m.
Walk-in-interview Venue: Lemon Tree Hotel, P4, Rajiv Gandhi Infotech Park, Phase 1, Hinjawadi, Pune 411057
Contact: 020 4423 2323

Interested candidates may also email their resume to hardikb.pandya@zyduscadila.com or send it by courier to the Human Resource Department, Cadila Healthcare Ltd., Sarkhej-Bavla NH-8A, Moraiya, Taluka-Sanand, Ahmedabad-382210 within 7 days.

Comments

Popular Posts in Last Month

Alembic Pharmaceutical ltd is Hiring

Urgent Vacancy in Alembic Pharma Alembic Pharmaceutical ltd is Hiring candidates, Alembic Pharmaceutical ltd with an established presence in the Indian Pharma industry has proud historical track record going back over 100 years. To realise our ambitious plans we call upon dynamic result oriented team members to join our API & formulation manufacturing unit locaed at PANELAV , near Vadodara Gujarat. Positions are:  Executive/ Sr.Executive/ Asst.manager/ dy.manager/Manager QC QA (formulation or API) For more information click on below image for zoom view. Get more Latest Job Details: Click on following link. Walk in interview in Quintiles on 1st october. Urgent Vacancy in Cliantha Research ltd 

Zydus Cadila: Walk-in Interview on 4th March 2017

Walk-in Interview for Zydus Cadila Vadodara on 04th March, 2017 Cadila Healthcare Limited Experience: 1 to 6 yrs Salary: INR 1,00,000 - 6,00,000 P.A Location: Vadodara/Baroda   Also Check  :  Urgent Vacancy in LUPIN and Mylan Department: Quality Assurance Qualification : M.Sc. Experience : 1 to 5 years of relevant experience in an API regulated plant. Job Description : Will be responsible for IPQA activities, QMS, and batch release, audit & compliance and qualification areas. Department: Quality Control: Qualification : M.Sc. Experience : 1 to 5 years of relevant experience in an API regulated plant. Job Description : Will be responsible for operation and documentation for chromatography & spectroscopy instruments and wet chemistry analysis for RM, IM & FP. Exposure to regulatory inspections & customer audits and working knowledge of analytical instrumentation related software and database is essential. Go...