Job Description

Who are we?

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!

• To perform analysis of stability samples of finished products, hold time samples of blend and in process samples and blend samples testing with prior experience 5-10 years.
• To perform analysis on the instruments such as IR, HPLC, GC, UV, UPLC and AAS, Potentiometer, KF Titrator and XRPD.
• Processing of the chromatographic data.
• To ensure Receipt, registration, Upkeep of samples and timely disposition.
• For timely reporting of Deviations and LIR (If any).
• For timely completion of Analytical Reports to adhere to Production schedules.
• To ensure that the analysis is Right first time.
• For timely review of Analytical Reports to adhere the Production schedules.
• For maintenance and upkeep of Sample storage area and reserve samples.
• To follow GMP, GLP practices at all times.
• Periodic preventive maintenance of the HPLC systems.
• To ensure compliance to Safety policies and Data integrity practices.
• To ensure that all activities undertaken are executed within the framework of good laboratory and documentation practices and the existing quality systems are adhered to.
• For any other responsibilities assigned by the reporting authority.

Qualifications

• Msc / Bsc in Chemistry with 5 to 10 years of experience in Quality Control department.

Function

Quality

Sub Function

Manufacturing Quality Control

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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.

Teva Pharmaceuticals