Job Title: Quality Analyst II
📅 Date Posted: September 16, 2025
📍 Location: Bangalore, India – 560064
🏢 Company: Teva Pharmaceuticals
🆔 Job ID: 63664
🌍 About Teva Pharmaceuticals
At Teva Pharmaceuticals, we’re united by a mission:
To make good health more affordable and accessible, helping millions around the world enjoy healthier lives.
As the world’s leading manufacturer of generic medicines, Teva’s portfolio includes numerous products featured on the World Health Organization’s Essential Medicines List. Every single day, more than 200 million people take one of our medicines.
With a presence in nearly 60 countries, Teva brings together diverse talent, backgrounds, and experiences. We are always seeking new ways to make a difference — and new people to join us on that journey.
🧭 Role Overview
The Quality Analyst II will ensure the highest standards of quality and compliance within Teva’s operations. This role demands deep knowledge of pharmaceutical quality systems, regulatory compliance, and computerized quality management tools.
🎯 Key Responsibilities
Apply in-depth knowledge of pharmaceutical quality and quality systems, aligned with global best practices.
Ensure compliance with cGxP requirements, Quality IT applications, and computer system validation and deployment.
Manage and execute complex quality-related activities across global and cross-functional teams.
Oversee and maintain Quality Management Systems (QMS) and Electronic Document Management Systems (EDMS).
Handle core QMS processes, including:
Deviations
CAPA (Corrective and Preventive Actions)
Laboratory investigations
Complaints
Trends
Change control
Document management
Notifications to Health Authorities and Management
Utilize tools such as Excel, Word, PowerPoint, MS Project, and SharePoint effectively.
Demonstrate strong initiative, resourcefulness, and a sense of urgency in meeting quality objectives and deadlines.
Communicate effectively — both verbally and in writing — in English.
(Preferred) Experience with Veeva Quality Systems.
🎓 Education & Experience
Required: Bachelor’s degree in Science.
Preferred: Advanced degree in Science, Regulatory Affairs, Computer Science, or Management.
Experience: 5–7 years in the pharmaceutical or related industry, with international and cross-functional exposure.
💻 Technical Skills
Strong command of MS Office Suite (Excel, Word, PowerPoint, Project).
Hands-on experience with EDMS and QMS platforms.
Familiarity with SharePoint for collaboration and documentation.
(Plus) Knowledge of Veeva Quality applications.
🧑🤝🧑 Internal Applicants
If you’re already part of Teva, please apply through the Internal Career Site (Employee Central) for priority consideration.
You can access the portal from your home network.
If you face login issues, reach out to your local HR/IT partner.
🌈 Equal Employment Opportunity (EEO) Commitment
Teva Pharmaceuticals is an Equal Opportunity Employer.
We value diversity, inclusion, and accessibility in our workplace.
Employment opportunities are provided without regard to:
Age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity/expression, ancestry, veteran status, national or ethnic origin, or any legally protected status.
If you require accommodations during the recruitment process, please inform us. All information will be treated confidentially and used solely to support your candidate experience.
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