3 - 7 years

0 Lacs

Posted:6 days ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

As a Jr. Executive at Teva Pharmaceuticals, you will play a crucial role in ensuring the quality of analytical documents, stability data, and various quality-related documents. Your responsibilities will include: - Reviewing quality-related analytical documents. - Reviewing and releasing stability data in software. - Preparing, reviewing, distributing, retrieving, controlling, and archiving quality documents. - Managing documents in Electronic Document Management System (EDMS). - Handling investigations and Corrective and Preventive Actions (CAPA). To excel in this role, you should have a minimum of 3 years of experience in Quality Control. Preference will be given to candidates familiar with handling Labware LIMS, Trackwise, Glorya, etc. Additionally, strong communication and interpersonal skills, good documentation practices, and computer literacy are essential qualifications for this position. At Teva Pharmaceuticals, we are on a mission to make good health more affordable and accessible, impacting millions of lives worldwide. Join us in our journey to continue making a difference and be a part of a diverse and passionate team dedicated to improving global healthcare. Apply now to be a part of our commitment to Equal Employment Opportunity.,

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Teva Pharmaceuticals logo
Teva Pharmaceuticals

Pharmaceutical Manufacturing

Tel-Aviv Petach Tikva

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