Quality Specialist II – Teva Careers | QA QC Jobs in Bangalore
Explore an exciting opportunity under Teva Careers as a Quality Specialist II, ideal for professionals seeking QA QC jobs and high-growth Pharma Jobs in Bangalore. This role at Teva Pharmaceuticals allows you to contribute to global healthcare through advanced Quality Management Systems, data-driven compliance activities, and continuous improvement across worldwide manufacturing sites.
Job Details:
- Job Title: Quality Specialist II
- Location: Bangalore, India, 560064
- Job Id: 64038
About the Company
Teva Pharmaceuticals, a global leader in generic medicines, is committed to making health more accessible and affordable. With a presence in nearly 60 countries and over 200 million people using Teva medicines daily, Teva Careers empowers professionals to make meaningful contributions to healthcare worldwide.
Job Description | Teva Careers
The Quality Specialist II role ensures timely and compliant completion of Product Quality Reviews (PQRs) and Annual Product Reviews (APRs). This position interacts with global manufacturing sites, quality units, and commercial teams, making it an excellent fit for talent seeking QA QC jobs and advanced Pharma Jobs in Bangalore.
Key Responsibilities:
PQR / APR Compilation & Coordination
- Complete Product Quality Reviews and Annual Product Reviews in a timely, compliant manner.
- Compile high-quality PQRs/APRs for products manufactured at various sites.
- Retrieve data from Quality and regulatory databases.
- Liaise globally with QA/QC, technical teams, and contract manufacturers.
- Recommend continuous improvement actions to quality units.
- Coordinate with supervisors, group leaders, and quality services teams.
- Manage data requests, follow-up with CMOs, and check quotations.
- Initiate PR/PO approvals for QPs.
- Schedule PQRs in SharePoint and maintain database updates.
- Escalate issues to PQR Centre management when required.
Quality Management Systems
- Initiate change controls and deviations.
- Prepare SOPs and related quality documentation.
- Participate in internal self-inspections.
Performance Management
- Contribute to continuous process improvement initiatives.
Training
- Prepare GMP training materials and impart procedural training.
Miscellaneous Support
-
Carry out additional assignments for ensuring team efficiency.
Qualifications Required For Teva Careers
- 2 to 8 years of experience in QA/QC within the pharmaceutical industry.
- Master’s or Bachelor’s degree in Pharmacy or natural sciences.
- Basic understanding of worldwide cGxP regulations.
- Strong English communication skills.
- Knowledge of computerised systems (TrackWise, SAP, LIMS, Global Insights, Glorya is an advantage).
- Understanding of manufacturing, QC, and contract manufacturing.
- Hands-on experience in analytical method development, validation, impurities, dissolution, and stability studies.
- Competence in reviewing qualification records and batch manufacturing documentation.
- Basic knowledge or experience in Product Quality Reviews.
Equal Employment Opportunity Commitment
Teva Pharmaceuticals ensures equal employment opportunities regardless of age, gender, ethnicity, disability, medical condition, or other protected characteristics. Accommodations are available throughout the recruitment process.
