Zydus Cadila is one of the Indias leading
healthcare companies and a global healthcare provider with a strength all along
the pharmaceutical value chain. The groups state-of-the-art manufacturing
infrastructure is spread across the five states Gujarat, Maharashtra, Goa,
Himachal Pradesh and Sikkim. Out of which, six facilities are USFDA approved.
The groups formulation manufacturing hub at Moraiya, Ahmedabad has received
approvals from the USFDA, MHRA of U.K., ANSM of France, MCC of South Africa,
ANVISA of Brazil to name a few.
If you have the talent and the zeal here is an opportunity for you to
join our manufacturing plant at Moraiya as:-
Executive / Senior Executive / Asst. Manager
CQA-LIMS M.Sc/M.Pharm with 4 to 8 years hands-on experience of HPLC, GC, Dissolution apparatus and UV Visible Spectrometer. Should have experience of review the analytical data (analytical work sheets and respective electronic data) related to Raw materials/Finished product and Stability, Calibration knowledge of QC Instruments (i.e. HPLC,GC,UV,IR,KF etc) , Knowledge of QMS and documentation, Audit trail review in related instrument software and review in LIMS.
Quality Assurance (OSD) B.Sc. /B.Pharm/M.Sc/M.Pharm with 2 to 6 Years of relevant experience of IPQA Activities for Tablets, Capsules, Pellets, Dry Powder/ Environment Monitoring in oral solid dosage manufacturing facilities.
For all the positions, candidate having exposure to regulatory requirement of documentation and cGMP/GLP is essential. Those with experience in SAP environment shall be preferred.
Interested candidates may Walk-in for an interview along-with their updated CVs and relevant documents as per below schedule.
Executive / Senior Executive / Asst. Manager
CQA-LIMS M.Sc/M.Pharm with 4 to 8 years hands-on experience of HPLC, GC, Dissolution apparatus and UV Visible Spectrometer. Should have experience of review the analytical data (analytical work sheets and respective electronic data) related to Raw materials/Finished product and Stability, Calibration knowledge of QC Instruments (i.e. HPLC,GC,UV,IR,KF etc) , Knowledge of QMS and documentation, Audit trail review in related instrument software and review in LIMS.
Quality Assurance (OSD) B.Sc. /B.Pharm/M.Sc/M.Pharm with 2 to 6 Years of relevant experience of IPQA Activities for Tablets, Capsules, Pellets, Dry Powder/ Environment Monitoring in oral solid dosage manufacturing facilities.
For all the positions, candidate having exposure to regulatory requirement of documentation and cGMP/GLP is essential. Those with experience in SAP environment shall be preferred.
Interested candidates may Walk-in for an interview along-with their updated CVs and relevant documents as per below schedule.
·
Date : Saturday, 01st December, 2018
·
Location : Ahmedabad
·
Timings : 10:00 AM 04:00 PM
·
Contact Person : Karn Singh
Interested Candidates may also email their resume to Karn.singh@zyduscadila.com or send it by courier to the
Human Resource Department, Cadila Healthcare Ltd., Sarkhej-Bavla NH-8A, Moraiya
Venue:
Cadila Healthcare Ltd,
Sarkhej-Bavla N.H.No. 8A,
Vill. - Moraiya, Tal. Sanand,
Dist: Ahmedabad,
Gujarat, India - 382210
helloo nov 1st 2018 malli ela vasthundhiii..koncham chusi update cheyandi
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