Applicatins are invited from B.pharma /M.pharma/B.sc/and M.sc students candidates with requites qualifaction for interview of vrarious posts.
B.sc /B.pharma/M.sc. with 2 to 8 years of hands on experience of HPLC ,GC,dissolution apparatus and UC-visible spectrometer .should also have knowledge of weight analysis ,stability studies for vaccines,injectables and oral solid dosage forms .
Quality assurance (OSD/injectable ):
M.sc /B.pharma with 1 to 8 year of relevant experience of IPQA activities /environment monitoring in vaccines /injectable manufacturing facilities .
corporate quality assurance -loan licensing:
B.pharma /M.pharma /M.sc with 4 to 12 year of hands on experience of audit of external vendors & internal audits (loan license sites & contract manufacturing sites ) of formulation .should also have sound knowledge of compliance and be well versed with QMS of mormulation (OSD ,injectable & liquid ).
for all above positions ,its is essential for candidates to have exposure to regulatory requirements of documentation and GMP/GLP. those with experience in SAP environment shall be preferred..
interested candidate may walk-in for an interview alogwith their CVs and relevant documents as per the folowing schedule.
informations to remember:
date : sunday ,22nd may 2016
location : indore
timings; 9:30A.M. to 5:00 p.m.
venue : hotel amar vilas ,1B , chandra nagar ,A.B.road ,indore madhya pradesh 452001
interested candidates may also email their resume to firstname.lastname@example.org or send it by courier to the human resouece deparment ,cadila healthcare Ltd.,sarkhej-bavla NH-8A ,moraiya ,taluka-sanad ,ahemdabad -382210 with in 7 days .
about the company :
zydus cadila is one of india's leading helthcare 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 state of gujrat ,maharashtra ,goa ,himanchal pradesh and sikkim. the group's fomulation manufacturing hub at moraiya ,ahmedabad has received approvals from several regulatory .