Quality Control Analyst I at Teva Pharmaceutical Industries Ltd. - Israel

, tamil nadu, India -

Full Time

Start Date

Immediate

Expiry Date

05 Feb, 26

Salary

0.0

Posted On

07 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Stability Analysis, Good Laboratory Practices, Good Documentation Practices, HPLC, UV Techniques, Chromatographic Data Interpretation, Analytical Activities Documentation, Data Integrity, Laboratory Software Handling, Safety Apparel Usage, Training Completion

Industry

Pharmaceutical Manufacturing

Description

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.How you’ll spend your day To perform Stability analysis. Maintenance of operating instruments / equipment. To maintain the assigned Laboratory workplace, instruments and equipment etc. To adhere Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure. Responsible for handling , operating and maintaining HPLC / UV and related instruments to ensure optimal performance. Adherence to Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure. Performing stability testing (Assay, RS & Dissolution) of all formulations by HPLC and UV techniques. Preparing samples and executing the same as per the Method of Analysis and Verification of sample set sequence in applicable software’s. Interpreting chromatographic data and ensuring proper documentation of all analytical activities in compliance with GLP / GDP requirements Reporting of interpreted data in line with specification, compliance and regulatory standards and maintaining data integrity throughout the analytical lifecycle. Evaluation of reported results and reporting of any abnormal results to the supervisor ontime. Handling of laboratory software's. Ensure to use safety apparels and PPEs while working in the laboratory. Ensure timely completion of assigned training. Your experience and qualifications M.Sc., Chemistry 7+ years of experience 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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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Responsibilities

The Quality Control Analyst I will perform stability analysis and maintain laboratory instruments and equipment. They will ensure adherence to Good Laboratory Practices and regulatory guidelines while conducting stability testing and interpreting chromatographic data.