Quality Assurance Jobs at Teva | Chemistry Jobs | Apply Now
The latest opportunity under Teva Careers is ideal for professionals looking for Quality Assurance Jobs in pharmaceutical manufacturing and compliance operations. This Bangalore-based role focuses on deviation investigations, cGMP compliance, CAPA systems, quality documentation, and regulatory inspections. Candidates interested in advanced Chemistry Jobs can gain strong industry exposure while working on pharmaceutical quality systems and global compliance operations in a leading biopharmaceutical company.
- Job Title: Quality Assurance Manager
- Location: Bangalore, India, 560064
- Job Id: 67711
About the Company:
Teva Pharmaceuticals is one of the world’s leading biopharmaceutical companies, known for innovative medicines and high-quality generics manufacturing. The company focuses on improving patient health through advanced pharmaceutical solutions in neuroscience, immunology, and healthcare. With a strong commitment to innovation, compliance, and operational excellence, Teva Careers provide excellent opportunities for professionals in pharmaceutical manufacturing, chemistry, quality assurance, and regulatory operations across global healthcare markets.
Job Overview:
The Quality Assurance Manager role focuses on maintaining pharmaceutical quality systems and ensuring compliance with cGMP regulations and company procedures. The selected candidate will manage deviation investigations, risk assessments, quality documentation, CAPA systems, and inspection readiness activities. The role also involves collaboration with affiliates, monitoring quality metrics, preparing reports, and supporting pharmaceutical manufacturing compliance operations within a regulated industry environment.
Key Responsibilities:
- Ensure compliance with cGMP directives and quality standards
- Lead deviation investigations and risk assessments
- Support CAPA systems and quality improvement initiatives
- Review and maintain quality documentation and SOPs
- Participate in regulatory and internal inspections
- Monitor quality metrics and KPI reporting
- Coordinate with affiliates regarding quality events
- Support pharmaceutical compliance operations
Educational Requirements:
- Master’s degree in chemistry, similar natural sciences, engineering or at least several years working experience in the quality assurance area.
- Experience in pharmaceutical manufacturing/validation/other related experience and/or in analytical control and regulatory compliance.
Skills Required:
- Understanding of the drug manufacturing process. Knowledge of generics and branded product development is a plus.
- Good interpersonal and communication skills, as well as organizational skills.
- Ability to communicate complex issues, decision-making, problem-solving skills.
- Proficient in written and spoken English.
- Proficiency in MS Office, SAP, Veeva.
This opportunity under Teva Careers is highly suitable for professionals aiming to build successful careers in Quality Assurance Jobs and pharmaceutical compliance. The role offers valuable experience in GMP operations, quality investigations, CAPA systems, and regulatory inspections within a global pharmaceutical environment. Candidates interested in long-term growth in Chemistry Jobs can gain strong technical expertise, leadership exposure, and professional development while contributing to healthcare and pharmaceutical quality excellence.
