Teva Pharmaceutical Industries Ltd. (also known as Teva Pharmaceuticals) is an Israeli multinational pharmaceutical company. Teva specializes primarily in generic drugs, but other business interests include branded-drugs, active pharmaceutical ingredients (API’s) and, to a lesser extent, contract manufacturing services and an out-licensing platform.
1.Vacancy details:
- Department: Quality Control Analyst II
- Qualifications: MSc / B Pharm, M Pharm
- Experience: 7 – 12 years
- Salary:₹ Not Disclosed
Job Description: Greeting from Teva Pharmaceuticals. ..!!!!
Important Details :
- Location: Chennai
- Post of date:11/05/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job description
Role & responsibilities
- 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 is in compliance with current guidelines
- Entry of stability sample results in LIMS
- Initiation of Quality forms in Track wise Harmony
- Handling of LSCMS Software
Preferred candidate profile
- MSc / B Pharm, M Pharm with 08-10 years of Experience in Stability Control
Email: [email protected]
2.Vacancy details:
- Department: Quality Control Technician III
- Qualifications:Masters/Bachelors Degree in Chemistry or equivalent degree
- Experience: 1 – 3 years
- Salary:₹ Not Disclosed
Job description
Role & responsibilities
- Calibration of HPLC, Gas Chromatography, Ion Chromatography, AAS, TOC, UV Spectrophotometer, FTIR, Raman, Potentiometer etc.
- Calibration of Dissolution Test Apparatus, UV Cabinet, Media Degasser etc.
- Standardization of KF Reagent.
- Timely completion of performance verification of instruments and equipment.
- Execution of instrument and equipment qualification protocols.
- Daily calibration of balances, pH meter, Conductivity meter, Dissolved Oxygen Meter.
- Preparation of reagents and standardization of volumetric solutions.
- Maintenance of spares/accessories of all laboratory instruments and equipment.
- Reporting of Deviations, Chromatographic Errors and LIR (If any).
- To follow Good Laboratory Practices and safety policies in the laboratory standard area.
- To ensure compliance to the policy and procedure requirements on Data integrity.
- Ensure maintenance of logbooks, Inspection lot number register and all relevant registers in the laboratory.
Qualification & Experience:
- 1-3 years of experience in Non-Routine section and calibration of laboratory instruments and equipment.
- Masters/Bachelors Degree in Chemistry or equivalent degree
Email:[email protected]
ABAC
