Ranbaxy Laboratories Limited (Ranbaxy), India's largest pharmaceutical company, is an integrated, research based, international pharmaceutical company, producing a wide range of quality, affordable generic medicines, trusted by healthcare professionals and patients across geographies. Ranbaxy today has a presence in 23 of the top 25 pharmaceutical markets of the world. The Company has a global footprint in 46 countries, world-class manufacturing facilities in 7 countries and serves customers in over 125 countries.
Post: Sr. Executive - Contract Manufacturing (Oral Liquids)
Job Description:
The incumbent will be responsible for overseeing the QA activities across Ranbaxy's contract manufacturing sites located in Gujarat Region.
Major areas of responsibilities would involve:
a. IPQA,
b. Master Vs. Working document review,
c. Ensure availability of valid master documents at site.
d. Ensure availability of working standards, columns and other accessories at site as part of
tech transfer.
e. Monitoring process validation
f. Batch release
g. Investigation related to market complaints, root cause identification and capa
implementation,
h. Investigation related to product recall, root cause identification and capa implementation,
i. Monitor Implementation of changes as per designated change control and closure of
document.
j. Deviation handling and their closure of document.
k. Handle local FDA and WHO audits along with site QA.
Desired Profile:
Applicants should have completed B. Pharm or M. Sc and must have 3- 5 years of relevant experience.
The incumbent could be based in any city in Gujarat and he/ she should be open to extensive travelling across Ranbaxy's contract manufacturing sites in Gujarat region.
Knowledge of local language will be an added advantage.
Additional Information:
Exp: 3-5 yrs
Location: Ahmedabad, Gandhinagar
Education: B.Pharm, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Production
END DATE: 15th oct, 2011
Forward your resume at, career@ranbaxy.com
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