Teva Pharmaceutical Recruiting For Quality Control Analyst II/Quality Control Technician III

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


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