QC/ QA Jobs in Bangalore: Teva Pharmaceuticals Is Hiring a Quality Specialist – Apply Now
Are you looking for QC/ QA Jobs in Bangalore to build your career? Teva Pharmaceuticals, a global leader in generic medicine manufacturing, is hiring for the position of Quality Specialist II in Bangalore, India. This role offers a dynamic opportunity to ensure compliance with global quality standards, review critical CMC documentation, and collaborate across Teva’s worldwide network. If you have a background in pharmacy, quality assurance, or analytical method development, this position provides the platform to contribute to one of the world’s most trusted healthcare brands.
About the Company:
Teva Pharmaceuticals is committed to making good health more affordable and accessible, helping millions worldwide lead healthier lives. As the leading manufacturer of generic medicines and a key producer of essential drugs listed by the World Health Organization, Teva’s products reach over 200 million people every day. With operations in nearly 60 countries and a diverse global workforce, we continuously seek innovative ways to make a difference — and new talent to help us achieve that mission. The Quality Specialist II ensures timely and compliant review of CMC documentation according to Teva corporate standards and guidelines. Responsibilities include reviewing Method Development and Validation Protocols, Stability Protocols and Reports, Instrument and Equipment Qualification records, and Batch Manufacturing Records. The role also oversees the compilation and approval of Product Quality Reviews (PQRs) and Annual Product Reviews (APRs) in coordination with manufacturing sites, global quality units, and commercial affiliates.
Job Details:
- Job Title: Quality Specialist II
- Location: Bangalore, India, 560064
- Job Id: 64031
Key Responsibilities:
1. Review of Documentation:
- Review CMC Documentation, Method Development, Validation protocols, and Stability Study reports.
- Review Instrument and Equipment Qualification records and Batch Manufacturing Records.
- Liaise with global QA/QC personnel to collect and organize required documentation and responses.
- Escalate issues to Supervisors or Managers as needed.
2. Product Quality Review (PQR) Compilation:
- Compile high-quality PQRs and APRs for products manufactured at various global sites.
- Retrieve data from quality and regulatory databases.
- Coordinate with third-party manufacturers for timely data collection.
- Prepare quotations, initiate PR/PO processes, and maintain PQR checklists in SharePoint.
3. Quality Management Systems:
- Initiate change controls and deviations.
- Prepare and maintain local SOPs and related documents.
- Participate in internal audits and self-inspections.
4. Performance and Training:
- Engage in continuous improvement projects for operational efficiency.
- Develop and deliver GMP and on-the-job training materials.
5. Miscellaneous Support:
-
Perform any additional tasks assigned by management to ensure smooth team functioning.
Education:
Master’s or Bachelor’s Degree in Pharmacy or related natural sciences.
Qualifications and Experience:
- 2–8 years of experience in QA/QC within the pharmaceutical industry.
- Basic understanding of global cGxP regulations and computerized systems (TrackWise, SAP, LIMS, etc.).
- Strong communication skills and proficiency in English.
- Hands-on experience in Analytical Method Development, Validation, Stability Studies, Instrument Qualification, and PQR review.
- Commitment to quality improvement and effective complexity management.
