Quality Assurance Specialist III

3 weeks ago


Gwalior, Madhya Pradesh, India Teva Pharmaceuticals Full time

About Us

Teva Pharmaceuticals is a global leader in the production of generic medicines, with a mission to make good health more affordable and accessible. Our diverse team of professionals works together to achieve this mission, with a strong commitment to quality and regulatory compliance.

Your Role

As a Quality Specialist III, you will be responsible for ensuring the timely dispatch of batches, verifying deviations and OOS/LIR, and reviewing documentation to ensure compliance with regulatory requirements. You will also be involved in investigations, corrective and preventive actions, and ensuring the effectiveness of these actions.

Responsibilities

  • Verify batch records, test results, and deviations to ensure compliance with regulatory requirements.
  • Review and approve documentation, including batch records, analytical data, and change controls.
  • Investigate and resolve deviations, OOS/LIR, and other quality-related issues.
  • Monitor and follow up on corrective and preventive actions to ensure timely closure.
  • Review and approve protocols and reports to determine the effectiveness of corrective and preventive actions.

Requirements

  • Bachelor's or Master's degree in a relevant field.
  • 3-4 years of relevant experience in quality assurance or control.
  • Hands-on experience in batch disposition, batch card review, and batch release.
  • Basic knowledge of deviation and OOS investigation.
  • Audit experience of USFDA, EDQM, EMA, TGA, or PMDA.
  • Experience with ERP, TrackWise, and LIMS systems.

Teva's Commitment to Diversity and Inclusion

Teva Pharmaceuticals is committed to equal opportunity in employment and diversity and inclusion. We strive to create a workplace that is inclusive and respectful of all employees, regardless of their background, culture, or identity.



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