Location: Bangalore, India, 560052
Date: February 19, 2025
Company: Teva Pharmaceuticals
Job ID: 58498
Are you passionate about ensuring quality in the pharmaceutical industry? Teva Pharmaceuticals, a global leader in generic medicines, is seeking a Quality Specialist III to join our team in Bangalore. This is an excellent opportunity to contribute to our mission of making good health more affordable and accessible worldwide.
About Teva Pharmaceuticals
At Teva, we are committed to improving the lives of millions by providing high-quality, affordable medicines. With a presence in nearly 60 countries, we take pride in being the world’s leading manufacturer of generic medicines and a key contributor to the World Health Organization’s Essential Medicines List. Every day, over 200 million people rely on our products, and we are constantly striving to make a greater impact.
The Opportunity
As a Quality Specialist III, you will play a critical role in ensuring the timely and compliant completion of Product Quality Reviews (PQRs) and Annual Product Reviews (APRs). Your work will directly contribute to maintaining the highest standards of quality for Teva’s products, manufactured across various global sites.
Key Responsibilities
- Data Compilation and Review:
- Compile high-quality APRs/PQRs for products manufactured at Teva sites and third-party contract manufacturers.
- Retrieve and analyze data from quality and regulatory databases.
- Liaise with global QA personnel and contract manufacturers to collect necessary data.
- Quality Management Systems:
- Initiate and manage change controls and deviations.
- Prepare and update local SOPs and related documents.
- Participate in self-inspection processes to ensure compliance.
- Performance Management:
- Engage in continuous process improvement projects to enhance efficiency.
- Recommend actions for quality improvement and communicate effectively with stakeholders.
- Training and Development:
- Prepare training materials for GMP and on-the-job training.
- Conduct training sessions as needed to ensure team compliance with procedures.
- Miscellaneous Support:
- Assist with additional tasks assigned by management to support team operations.
Qualifications and Experience
- Education: Master’s or Bachelor’s degree in Pharmacy or other natural sciences.
- Experience: 1 to 3 years of experience in QA/QC within the pharmaceutical industry.
- Skills:
- Basic knowledge of worldwide cGxP regulations.
- Proficiency in English; additional language skills are a plus.
- Strong communication and interpersonal skills.
- Familiarity with computerized systems such as TrackWise, SAP, LIMS, and Global Insights is advantageous.
- Hands-on experience in PQR compilation is preferred.
