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Teva Pharmaceuticals Hiring for Quality Specialist

About Teva Pharmaceuticals

Teva Pharmaceuticals is a global leader in generic medicines and healthcare solutions, operating in nearly 60 countries. Teva is dedicated to making affordable, quality healthcare accessible worldwide, with a portfolio that serves over 200 million people globally every day. Join our mission to improve lives through medicines listed on the World Health Organization’s Essential Medicines List. Teva Pharmaceuticals Hiring for Quality Specialist


Job Title: Quality Specialist III

Location: Bangalore, India, 560052
Experience Required: 1–3 Years
Salary: 4.5–5 LPA
Qualifications: B.Pharm, M.Pharm, BSc, MSc


Key Highlights

  • Verified Job
  • Work-life balance and flexibility
  • Time management and problem-solving opportunities

Responsibilities

As a Quality Specialist III, you will:

A. Data Requesting and PQR Compilation

  • Prepare Annual Product Reviews (APRs) and Product Quality Reviews (PQRs) for Teva’s products.
  • Retrieve data from quality and regulatory databases.
  • Coordinate with third-party contract manufacturers and global QA teams for timely data collection.
  • Update records in the SharePoint database and escalate issues when needed.

B. Quality Management Systems

  • Initiate processes for change controls and deviations.
  • Draft and manage local SOPs and related documentation.
  • Participate in internal self-inspections to ensure compliance with quality standards.

C. Performance Management

  • Engage in continuous process improvement projects to enhance efficiency and quality.

D. Training

  • Develop training materials for Good Manufacturing Practices (GMP).
  • Conduct on-the-job training for team members.

E. Miscellaneous Support

  • Handle additional tasks assigned by management to ensure smooth team operations.
Teva Pharmaceuticals Hiring for Quality Specialist
Teva Pharmaceuticals Hiring for Quality Specialist

Qualifications

To be eligible for the role, candidates should meet the following criteria:

Education

  • A Bachelor’s or Master’s degree in Pharmacy or Natural Sciences.
See also  Fresher Augmedix Hiring for Medical Documentation Specialist

Experience

  • 1–3 years in a QA/QC role within the pharmaceutical industry.

Knowledge

  • Basic understanding of worldwide cGxP regulations.
  • Familiarity with manufacturing, QC, and contract manufacturing processes.

Preferred Skills

  • Experience with PQR compilation.
  • Proficiency in IT systems like TrackWise, SAP, LIMS, and Global Insights.

Required Skills

  • Excellent communication skills in English (knowledge of additional languages is a plus).
  • Basic computer knowledge.
  • Strong ability to manage complex processes and drive quality improvements.

How to Apply

Interested candidates can apply online through the Teva Pharmaceuticals careers portal.

This is a great opportunity for professionals looking to excel in quality management within the pharmaceutical industry.

Apply today and become a part of Teva Pharmaceuticals, where your expertise makes a global impact! Teva Pharmaceuticals Hiring for Quality Specialist

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Teva Pharmaceuticals Hiring for Quality Specialist
Teva Pharmaceuticals Hiring for Quality Specialist
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