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Teva Pharmaceuticals Quality Control Analyst Opening/Job

 Teva Pharmaceuticals Quality Control Analyst Opening/Job



Quality Control Analyst 
Location:  Chennai, India, 600113
Company:  Teva Pharmaceuticals
Job Id:  49075

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

-- Has limited discretion to vary from established procedures -- Has limited work experience involving basic concepts and procedures -- Works under general supervision -- Performs routine assignments in the entry level of the Professional Career Band -- Typically requires a college or university degree or the equivalent work experience that provides knowledge and exposure to fundamental theories, principles and concepts -- Develops competence by performing structured work assignments -- Uses existing procedures to solve routine or standard problems -- Receives instruction, guidance and direction from others

How you’ll spend your day
Performing Stability analysis and review of documents.
Performing Method transfer/ Method Validation
Calibration and validation of instruments / equipment’s.
Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelines.

Preparation of departmental SOP’s in compliance with current guidelines.

Preparation of validation protocols in compliance with current guidelines.
Entry of stability sample results in LIMS.
Handling of LSCMS Software.

Your experience and qualifications
M.Sc., (Chemistry) with 5 to 10 years of experience.
Good communication skill.
Possess a pro-active, dynamic and flexible approach .
Enjoy a more rewarding choice
Make a difference with Teva Pharmaceuticals
Reports To
In process of validation

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: Internal Career Site

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.





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