A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post: Associate QA Manager
Job Description
Perform review of GMP relevant documents such as analytical raw data, analytical methods etc. for compliance with SOPs/ Guidelines etc. Negotiate GMP deficiencies with Line Unit. Recognises complex deficiencies in the GMP documents and reports to the supervisor Writes and complete GMP relevant documents in own area of responsibility. Participate in training and coaching the new employees of Line unit with respect to GMP aspects Assures Lifecycle of Equipment / Facility and Computerized Systems corresponds to requirements are appropriately implemented and followed.
Review Stability Study records, Protocols and Reports for Drug Substance and Drug Products. Approve Deviation management and Change control for premises/facilities and equipment, IT systems and Analytical Documentation. Carry out internal audits as well as vendor/supplier audits. Manage daily operation and complete the task as per require TAT.
Master Degree English Relavant Experience in Slotted Dev & Med
Additional Information:
Job ID: 133853BR
Experience: 2-3 Year
Industry Type: Pharma/Biotech/Clinical Research
Location: Hyderabad
Functional Area: QA
End Date: 15th Jan, 2014
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