Location: Bangalore, India
Company: Teva Pharmaceuticals
Position: Regulatory Affairs Associate II
Job Type: Full-time
Experience Required: Minimum 3 years
Application Mode: Online
About Teva Pharmaceuticals
Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines with a strong presence in over 60 countries. Known for innovation, research excellence, and a mission to improve patient health, Teva continues to impact millions of lives worldwide.
This opening is for a Regulatory Affairs Associate II position in Bangalore, India, focusing on Canadian regulatory labeling and compliance with Health Canada guidelines. Teva Pharma Hiring Regulatory Affairs Associate II
Job Overview
The Regulatory Affairs Associate II role is designed for professionals with expertise in Canadian labeling regulations and regulatory submissions. The position involves close collaboration with global teams to ensure timely and accurate compliance with Health Canada requirements. Teva Pharma Hiring Regulatory Affairs Associate II
If you are a Pharma Graduate or Postgraduate with experience in regulatory affairs, labeling, and eCTD submissions, this opportunity offers growth, stability, and global exposure.
Key Responsibilities
As a Regulatory Affairs Associate II, your primary duties include: Teva Pharma Hiring Regulatory Affairs Associate II
| Responsibility | Details |
|---|---|
| Health Canada Updates | Review monthly Health Canada brand safety updates and align with company product lists. |
| Labeling Changes | Strategize labeling modifications impacting multiple product documents. |
| Product Monographs | Retrieve, update, and maintain product monographs (PMs) using Health Canada Drug Product Database. |
| Template Compliance | Ensure alignment with HC master templates through validation tools such as TVT. |
| Bilingual Labeling | Coordinate with French translators for bilingual packaging components. |
| Proofreading & QC | Conduct quality checks for labeling and submission documents. |
| Regulatory Commitments | Support Level III safety updates and other regulatory commitments. |
| Health Canada Queries | Manage clarifaxes, BA/BE queries, withdrawals, and extension requests. |
| Submission Management | Maintain trackers, project timelines, and ensure timely eCTD-compliant submissions with Regulatory Operations. |
| Compliance Updates | Stay informed about evolving Health Canada regulations and update processes accordingly. |
Required Qualifications
To be successful in this role, you must have: Teva Pharma Hiring Regulatory Affairs Associate II
- Educational Background: Pharma Graduate or Post Graduate in a scientific or regulatory discipline.
- Experience: Minimum 3 years of regulatory affairs experience with a focus on Canadian labeling.
- Technical Knowledge: Strong understanding of Health Canada labeling requirements.
- Tools & Skills: Experience in XML/SPM development and Canadian submissions.
- Work Approach: Ability to work independently with minimal supervision.
- Attention to Detail: Strong proofreading and documentation review skills.
Preferred Skills
- Knowledge of eCTD submission structure and regulatory operations.
- Familiarity with electronic labeling systems and data management tools.
- Strong organizational and time-management skills to handle multiple priorities.
- Excellent communication skills for cross-functional collaboration.
Benefits of Working at Teva Pharmaceuticals
Working at Teva offers more than just a career opportunity. It provides a chance to be part of a global healthcare leader committed to innovation, patient safety, and regulatory excellence. Teva Pharma Hiring Regulatory Affairs Associate II
Some benefits include:
- Exposure to international regulatory frameworks, especially Health Canada labeling requirements.
- Professional growth in a collaborative and diverse workplace.
- Equal employment opportunity and inclusivity in the work culture.
- Opportunities to work on projects impacting millions of patients worldwide.
- Access to continuous learning and development programs.
Why Choose a Career in Regulatory Affairs at Teva?
A role in regulatory affairs at Teva provides professionals with a unique opportunity to influence product safety and compliance on a global scale. By ensuring accurate labeling, compliance with evolving regulations, and timely submissions, you will contribute directly to patient safety and healthcare innovation. Teva Pharma Hiring Regulatory Affairs Associate II
This position in Bangalore allows you to gain international experience while working closely with global teams, making it an ideal career choice for ambitious regulatory professionals.
Career Growth Opportunities
Teva provides structured career development pathways. As a Regulatory Affairs Associate II, you can expect: Teva Pharma Hiring Regulatory Affairs Associate II
- Opportunities to advance to Senior Regulatory Affairs roles.
- Exposure to cross-functional projects with R&D, Quality, and Manufacturing teams.
- Specialized training in international regulatory frameworks.
- Long-term career stability with one of the world’s most respected pharmaceutical companies.
Job Location
- City: Bangalore, Karnataka, India
- Work Mode: Office-based with collaboration across global teams
Application Process
Interested candidates can apply online through Teva’s official career portal. Teva Pharma Hiring Regulatory Affairs Associate II
How to Apply:
- Visit the official application link (Teva Careers Portal).
- Register or log in to your Teva account.
- Fill in the required details and upload your updated resume.
- Submit your application before the deadline.
Summary Table
| Job Title | Regulatory Affairs Associate II |
|---|---|
| Company | Teva Pharmaceuticals |
| Location | Bangalore, India |
| Published On | October 1, 2025 |
| Qualification | Pharma Graduate / Post Graduate in a scientific or regulatory background |
| Experience | Minimum 3 years |
| Specialization | Canadian regulatory labeling, Health Canada compliance |
| Application Mode | Online |
Final Thoughts
This is an excellent opportunity for regulatory professionals with experience in Canadian labeling to join a global pharmaceutical leader. The role not only ensures compliance with Health Canada regulations but also contributes to patient safety and international product success. Teva Pharma Hiring Regulatory Affairs Associate II
If you are motivated, detail-oriented, and passionate about regulatory affairs, apply now to build a rewarding career at Teva Pharmaceuticals.
Teva Pharmaceuticals hiring Regulatory Affairs Associate II in Bangalore with 3+ years Canadian labeling experience. Apply online for global opportunity.
