Kemwell Pvt Ltd., established in the year 1972 at Bangalore, Specializes in contract manufacturing for pharmaceutical formulations for various reputed multinations in India. For its expansion plans is looking for yound dynamic personnel.
Post: Manager Validation-QA
Responsible to set up a Validation Team.Preparation and execution of protocols for media fill validation activities for Filling line and media hold studies for Bioreactors and Vessels. Candidate must have 2-3 years work experience in biotech field.
To Plan and coordinate all the Validation Activities.In-depth understanding of Regulatory Requirements.Exposure to HVAC, clean utility and facility Qualification and Validation.First hand exposure to regulatory audits – USFDA, EMEA, TGA, MCC etc.
Experience: 8-10 Years
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QA, QC
End Date: 15th July, 2011
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