Job Description
- 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
Candidate Profile
• Must have 3-5 years of work experience in Quality Control Formulations
• Must be a Post Graduate in Industrial Chemistry/B.Pharm or M.Sc
• Must possess good communication skills and be performance driven
• Should have knowledge of dissolution tester with auto sampler, UV-Visible spectrophotometer, HPLC with Empower 3 software
• Must have 3-5 years of work experience in Quality Control Formulations
• Must be a Post Graduate in Industrial Chemistry/B.Pharm or M.Sc
• Must possess good communication skills and be performance driven
• Should have knowledge of dissolution tester with auto sampler, UV-Visible spectrophotometer, HPLC with Empower 3 software
Additional Information
Experience : 3-5 years
Qualification : M.Sc, B.Pharm
Location : Chennai
Industry Type : Pharma
Functional Area : Quality
End Date : 5th January, 2019
Experience : 3-5 years
Qualification : M.Sc, B.Pharm
Location : Chennai
Industry Type : Pharma
Functional Area : Quality
End Date : 5th January, 2019
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