WhatsApp Group Join Now
Telegram Group Join Now

Teva Pharma1

1 - 3 Years

4.5 - 5 LPA

Bangalore, India, 560052

B.Pharm, Bsc, M Pharm, Msc

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Teva Pharmaceuticals, a global leader in generic medicines and healthcare solutions, is dedicated to making quality healthcare affordable and accessible worldwide. With operations in nearly 60 countries, Teva takes pride in its mission to improve lives by producing medicines listed on the World Health Organization’s Essential Medicines List. Join a workforce where over 200 million people globally rely on its products every day.

Responsibilities in the Job

As a Quality Specialist III at Teva Pharmaceuticals in Bangalore, you will play a crucial role in maintaining and improving the company’s quality management processes. Your primary duties include:

A. Data Requesting and Compilation of PQRs

  • Preparing high-quality Annual Product Reviews (APRs) and Product Quality Reviews (PQRs) for Teva’s products.
  • Retrieving data from quality and regulatory databases.
  • Coordinating with third-party contract manufacturers and global QA teams for timely data collection.
  • Updating records in the SharePoint database and escalating issues when necessary.

B. Quality Management Systems

  • Initiating processes for change controls and deviations.
  • Drafting and managing local SOPs and related documentation.
  • Participating in internal self-inspections to uphold quality standards.

C. Performance Management

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

D. Training

  • Developing training materials for GMP (Good Manufacturing Practices) and conducting on-the-job training for team members.

E. Miscellaneous Support

  • Handling additional tasks assigned by management to ensure smooth team operations.

Qualifications

Candidates applying for this role must meet the following criteria:

  • Education: A Master’s or Bachelor’s degree in Pharmacy or natural sciences.
  • Experience: 1 to 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 Teva IT systems such as TrackWise, SAP, LIMS, and Global Insights.

Skills

  • Excellent communication skills in English (additional languages are an advantage).
  • Basic knowledge of computer systems.
  • Ability to manage complexity and drive quality improvements.

Application Link

Sticky Buttons
Join WhatsApp Group References Join Telegram