Quality Assurance Jobs | TEVA is Hiring | Life Sciences Graduates Apply Now
Looking for high-paying Quality Assurance Jobs in the pharmaceutical industry? Teva Pharmaceuticals is hiring experienced professionals for the role of Quality Assurance Manager in Bangalore. This is an excellent opportunity for candidates from engineering, and life sciences backgrounds to build a career with one of the world’s leading biopharmaceutical companies. Candidates with expertise in GMP compliance, deviation management, CAPA, and regulatory compliance can explore this exciting Teva Careers opportunity today.
- Job Title: Quality Assurance Manager
- Location: Bangalore, India, 560064
- Job Id: 67711
About the Company
Teva Pharmaceuticals is a globally recognized biopharmaceutical company known for its innovative medicines and world-class generics business. The company operates across multiple healthcare segments including neuroscience, immunology, and pharmaceutical manufacturing. Teva focuses on delivering high-quality medicines worldwide while maintaining strong regulatory and compliance standards. With a collaborative and inclusive work culture, the company provides employees with opportunities for professional growth, flexible work environments, and global exposure. Teva Careers continues to attract skilled professionals from pharmacy and life sciences backgrounds worldwide.
Key Responsibilities
- Ensure compliance with all applicable cGMP directives, regulations, and guidelines to maintain the high quality of pharmaceutical products.
- Lead and oversee deviation investigations, ensuring compliance with Teva corporate procedures and local quality procedures.
- Perform impact and risk assessments for critical quality events.
- Assess and categorize deviations and determine the impact on affected batches.
- Coordinate with Teva affiliates regarding deviations that may affect product deliveries.
- Review and evaluate deviation reports from contract manufacturers, assessing their potential impact on the batch release process in collaboration with the responsible Teva release QP.
- Participate in regulatory inspections, Teva corporate inspections, and internal self-inspections within the scope of responsibility.
- Collect and analyse quality data and documentation, prepare documentation packages for Quality Alignment Meetings (QAMs) and Market Action Committees (MACs) in accordance with approved templates, and prepare Health Authority (HA) notification letters.
- Monitor and trend deviations and quality metrics to identify improvement opportunities.
- Prepare and report KPIs related to quality events and deviation management.
- Author and maintain local SOPs related to critical quality issues, deviation management, CAPA, and CAPA effectiveness.
Education
Master’s degree in natural sciences, engineering or at least several years of working experience in the quality assurance area.
Skills
- Experience in pharmaceutical manufacturing/validation/other related experience and/or in analytical control and regulatory compliance.
- 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.
If you are looking for stable and growth-oriented Quality Assurance Jobs in the pharmaceutical sector, this Teva Careers opportunity can be an excellent step forward. With exposure to global pharmaceutical operations, regulatory systems, and quality compliance practices, candidates from pharmacy and life sciences backgrounds can build a rewarding professional career at Teva Pharmaceuticals. Interested applicants are encouraged to apply online at the earliest.
