Share this Job

Quality Control Analyst I

Date: Mar 15, 2019

Location: Chennai, IN, 600113

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.  This is how we improve health and enable people to live better, healthier lives.  Join us on our journey of growth!

Job Description

Job Description: Quality Control Analyst I

Role and Responsibilities: 

  1. Performing Stability analysis, Method transfer and Method Validation.
  1. Preparation and review of Method Transfer Protocols, Standard Testing Procedure, Specifications, Test Data Sheet 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. Review and maintenance of  all logbooks of  the department
  1. Preparation of departmental SOP’s in compliance with current guidelines. Review of departmental SOP’s, training of analysts and other technical staff and review validation of data transfer, data management using computer systems.
  1. Preparation and review of validation protocols in compliance with current guidelines.
  1. Calibration and validation of all instruments / equipments.
  1. Procurement of columns, chemicals/ reagents/ solvents and standards for various stability analysis, method transfer and method validations.

 

Function

Quality

Qualifications

  1. Must have prior experience in analysis stability, finished samples handling of HPLC, GC and Dissolution.
  2. Ability to be performance/target/goal oriented.
  3. Must have 4- 7 years of work experience in Quality Control Formulations
  4. Must be a Post Graduate in Industrial Chemistry/B.Pharm or M.Sc.
  5. Must possess good communication skills and be performance driven
 

Sub Function

Manufacturing Quality Control

Reports To

In process of validation

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.