Quality Control Analyst II

11 - 15 years

0 Lacs

Posted:1 week ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Role Overview: As a Quality Control Analyst II at Teva Pharmaceuticals, you will be responsible for performing Stability analysis, Method transfer, Method Validation, and reviewing analytical documents. Your main tasks will include preparation and review of Method Transfer Protocols (MTP), Method transfer report (MTR), Method of analysis (MTH), Standard Testing Procedure, Test Data Sheet (TDS) for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports, and any document related to stability analysis, method transfer, and method validation in compliance with current guidelines. Additionally, you will be involved in the review and maintenance of all logbooks of the department, preparation of departmental SOPs, calibration and validation of instruments/equipments, and entry of stability sample results in LIMS & SAP. You will also handle LSCMS software and initiate Quality Forms in Trackwise Harmony, documents in Glorya EDMS, and CAPA in Trackwise Harmony. Key Responsibilities: - Perform Stability analysis, Method transfer, Method Validation, and review of analytical documents - Prepare and review Method Transfer Protocols, Method transfer report, Method of analysis, Standard Testing Procedure, Test Data Sheet for Stability Analysis, Method transfer, and Method Validation - Review and maintain all logbooks of the department - Prepare departmental SOPs and review validation of data transfer, data management - Calibration and validation of all instruments/equipments - Entry of stability sample results in LIMS & SAP - Handle LSCMS software - Initiate Quality Forms in Trackwise Harmony, documents in Glorya EDMS, and CAPA in Trackwise Harmony Qualifications Required: - M. Pharmacy degree - Minimum 10 years and 7 months of experience Additional Company Details: Teva Pharmaceuticals is on a mission to make good health more affordable and accessible globally. They are the world's leading manufacturer of generic medicines and produce many products on the World Health Organization's Essential Medicines List. With at least 200 million people around the world taking their medicines daily, Teva Pharmaceuticals is constantly looking for new ways to make a difference and welcomes individuals who share their passion for improving global health. Role Overview: As a Quality Control Analyst II at Teva Pharmaceuticals, you will be responsible for performing Stability analysis, Method transfer, Method Validation, and reviewing analytical documents. Your main tasks will include preparation and review of Method Transfer Protocols (MTP), Method transfer report (MTR), Method of analysis (MTH), Standard Testing Procedure, Test Data Sheet (TDS) for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports, and any document related to stability analysis, method transfer, and method validation in compliance with current guidelines. Additionally, you will be involved in the review and maintenance of all logbooks of the department, preparation of departmental SOPs, calibration and validation of instruments/equipments, and entry of stability sample results in LIMS & SAP. You will also handle LSCMS software and initiate Quality Forms in Trackwise Harmony, documents in Glorya EDMS, and CAPA in Trackwise Harmony. Key Responsibilities: - Perform Stability analysis, Method transfer, Method Validation, and review of analytical documents - Prepare and review Method Transfer Protocols, Method transfer report, Method of analysis, Standard Testing Procedure, Test Data Sheet for Stability Analysis, Method transfer, and Method Validation - Review and maintain all logbooks of the department - Prepare departmental SOPs and review validation of data transfer, data management - Calibration and validation of all instruments/equipments - Entry of stability sample results in LIMS & SAP - Handle LSCMS software - Initiate Quality Forms in Trackwise Harmony, documents in Glorya EDMS, and CAPA in Trackwise Harmony Qualifications Required: - M. Pharmacy degree - Minimum 10 years and 7 months of experience Additional Company Details: Teva Pharmaceuticals is on a mission to make good health more affordable and accessible globally. They are the world's leading manufacturer of generic medicines and produce many products on the World Health Organization's Essential Medicines List. With at least 200 million people around the world taking their medicines daily, Teva Pharmaceuticals is constantly looking for new ways to make a difference and welcomes individuals who share their passion for improving global health.

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Teva Pharmaceuticals logo
Teva Pharmaceuticals

Pharmaceutical Manufacturing

Tel-Aviv Petach Tikva

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