QA QC Jobs | Teva is Hiring Life Sciences Candidates | Apply Now
Looking for high-paying QA QC Jobs in the pharmaceutical industry? The latest Teva Careers opportunity in Bangalore is now open for professionals interested in quality assurance, GMP compliance, supplier qualification, and pharmaceutical operations. This role is an excellent opportunity for candidates seeking stable and growth-oriented Life Sciences Jobs in a global biopharmaceutical company.
- Job Title: 3rd Party Quality Operations Manager – ExM 1
- Location: Bangalore, India
- ID: 67713
About the Company
Teva Pharmaceuticals is one of the world’s leading biopharmaceutical companies known for its innovative medicines and global generics business. The company focuses on improving healthcare accessibility and delivering high-quality pharmaceutical products worldwide. Teva offers strong career growth, global exposure, and advanced pharmaceutical operations experience for candidates pursuing long-term Life Sciences Jobs and QA QC Jobs.
Key Responsibilities
- Manage pharmaceutical products throughout their lifecycle to ensure quality and regulatory compliance.
- Coordinate quality-related activities with cross-functional expert teams.
- Act as a key contact for pharmaceutical quality issues related to third-party manufactured products.
- Coordinate GMP documentation related to manufacturing, QC, and QA processes.
- Support Quality Relationship Management and supplier quality activities.
- Initiate, coordinate, and evaluate product changes and new product introductions (change control).
- Maintain supplier regulatory compliance and Approved Vendor Lists in line with EMA requirements.
- Support supplier qualification, QA due diligence, audits, and inspections for contract manufacturers.
- Review and authorize master documents including CoA, specifications, batch records, analytical methods, and stability schedules.
- Support preparation, negotiation, review, and approval of Quality Technical Agreements (QTAs).
- Assist in audit preparation, technical visits, and supplier inspection readiness activities.
- Support Product Quality Reviews (PQRs) and ensure portfolio inclusion in PQR planning.
- Participate in deviation investigations and management of critical quality incidents.
- Support SOP creation, maintenance, and compliance with Teva standards and regulations.
- Perform additional quality and compliance responsibilities as assigned.
Qualifications
- Bachelor’s degree in Natural/Engineering science or related field.
- 3+ years’ experience in quality control/analysis, production and/or quality assurance.
Skills
- Must have working knowledge of cGMPs and applicable international regulations/guidelines.
- Strong computer skills including MS Office, TrackWise, and SAP.
- Good communication skills and resilience.
- Good command of the written and spoken English language.
This Teva Careers opportunity is ideal for candidates seeking advanced QA QC Jobs in the pharmaceutical industry. With exposure to GMP systems, audits, supplier management, and regulatory compliance, this role can significantly strengthen your professional journey in Life Sciences Jobs and pharmaceutical quality operations.
