Pharma Quality Specialist Role at Teva Pharma – Apply Now
Quality Specialist III
Date: Dec 2, 2024
Location: Bangalore, India, 560052
Company: Teva Pharmaceuticals
Job Id: 58499
Who we are
Together, we’re on a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. Our diverse team spans nearly 60 countries, making us the world’s leading manufacturer of generic medicines and a producer of products listed on the World Health Organization’s Essential Medicines List. At least 200 million people globally rely on our medicines daily.
The opportunity
- Ensures timely and compliant completion of Product Quality Reviews (PQRs) / Annual Product Reviews (APRs) as per Teva’s CORP Quality Management Systems.
- Collaborates with Teva Manufacturing Sites, Global Quality Units, and Commercial Affiliates to meet targets and ensure compliance.
- Responsibilities include compiling high-quality PQRs/APRs, retrieving data from Quality and Regulatory databases, and liaising with global third-party contract manufacturers and QA personnel.
- Recommends actions for continuous improvement in product quality and communicates professionally with relevant stakeholders.
- Reports to Supervisor, Group Leader, Manager Global Quality Services, and other managerial entities in Quality Strategy & Shared Services.
How you’ll spend your day
- Data Requesting and Compilation of PQRs:
- Compile high-quality PQRs/APRs for various manufacturing sites.
- Retrieve data from Quality and Regulatory systems.
- Liaise with third-party manufacturers and QA personnel for data collection.
- Follow up with CMOs for timely receipt of data.
- Verify quotations from CMOs and initiate PR/PO for QP’s approval.
- Maintain PQR receipt checklist and schedule PQRs in SharePoint.
- Escalate PQR issues as needed.
- Update the SharePoint database contemporaneously.
- Quality Management Systems:
- Initiate change controls and deviations processes.
- Prepare local SOPs and related documents.
- Participate in self-inspections.
- Performance Management:
- Engage in process improvement projects to enhance efficiency.
- Training:
- Develop training materials for GMP and on-the-job training.
- Provide training as required.
- Miscellaneous Support:
- Undertake additional tasks as assigned for smooth team operations.
Your experience and qualifications
Experience: 1 to 3 years in QA/QC function in the pharmaceutical industry.
Education: Master’s Degree in Pharmacy or other natural sciences, or Bachelor’s Degree in Pharmacy or other natural sciences.
Skills and Knowledge:
- Basic understanding of worldwide cGxP regulations.
- Proficiency in English; additional language skills are an advantage.
- Strong communication skills.
- Basic knowledge of computerized systems. Familiarity with systems in Teva’s IT landscape (e.g., TrackWise, SAP, LIMS, Global Insights, Glorya) is beneficial.
- Knowledge of manufacturing, QC, and contract manufacturing processes.
- Ability to drive improvements and manage complexity.
- Hands-on experience in PQR compilation is preferred.
Reports To: Group Leader, Quality Assurance
Keywords: Teva Pharma, Quality Specialist III, Pharmaceutical Industry, QA, QC, GMP Training, Quality Management Systems, Bangalore, India. Pharma Quality Specialist Role at Teva Pharma – Apply Now. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.
