• Performing Stability analysis and review of documents.
• Performing Method transfer/ Method Validation.
• Calibration and validation of instruments / equipments
• Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Specifications (SPEC), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation, Analytical Report (AR) any document related to stability analysis, method transfer / method validation in compliance with current guidelines.
• Preparation of departmental SOP’s in compliance with current guidelines
• Preparation of validation protocols in compliance with current guidelines
1) Must have 1-2 years of work experience in Quality Control Formulations
2) Must be a Post Graduate in Industrial Chemistry/B.Pharm or M.Sc
3) Must possess good communication skills and be performance driven
4) Should have knowledge of dissolution tester with auto sampler, UV-Visible spectrophotometer, HPLC with Empower 3 software
Experience : 1-2 years
Qualification : M.Sc, B.Pharm
Location : Chennai
Industry Type : Pharma
Functional Area : Quality Control
End Date : 10th January, 2019
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