Quality Control Analyst I
Teva Pharmaceutical Industries
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How you’ll spend your day
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Performing Stability analysis and review of documents
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Performing Method transfer/ Method Validation
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Calibration and validation of instruments / equipment’s
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Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelines
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Preparation of departmental SOP’s in compliance with current guidelines
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Preparation of validation protocols in compliance with current guidelines
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Entry of stability sample results in LIMS
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Handling of LSCMS Software
Your experience and qualifications
- M.Sc(Chemistry) with 5 to 10 years of experience
Teva’s Equal Employment Opportunity Commitment
This job is no longer accepting applications
See open jobs at Teva Pharmaceutical Industries.See open jobs similar to "Quality Control Analyst I" Greatness.bio.