Are you a detail-oriented professional with a passion for regulatory compliance and pharmaceutical labelling? Teva Pharmaceuticals, a global leader in generic and speciality medicines, is hiring for the position of Regulatory Affairs Associate II at its Bangalore office. This full-time opportunity is ideal for individuals with experience in Canadian regulatory labelling and a strong understanding of Health Canada guidelines.
📍 Job Details
Job Title: Regulatory Affairs Associate II
Location: Bangalore, India – 560064
Company: Teva Pharmaceuticals
Job ID: 62833
Date Posted: October 1, 2025
Employment Type: Full-Time
🌟 About Teva Pharmaceuticals
Teva is committed to making affordable and accessible healthcare a reality for millions across the globe. With operations in nearly 60 countries and a portfolio that includes many products listed on the World Health Organisation’s Essential Medicines List, Teva impacts over 200 million lives daily. Working at Teva means being part of a mission-driven organisation that values diversity, innovation, and excellence.
🎯 Role Overview
The Regulatory Affairs Associate II will support Canadian regulatory labelling activities, ensuring compliance with Health Canada’s safety updates and documentation standards. This role involves managing product monographs, coordinating bilingual labelling components, and collaborating with cross-functional teams to maintain regulatory accuracy and efficiency.
🔍 Key Responsibilities
Monitor monthly Health Canada safety updates and align them with internal product lists.
Create and update Product Monographs (PMs) by referencing Canadian innovator products.
Use tools like TVT for document comparison and ensure alignment with Health Canada templates.
Coordinate bilingual PMs with French translators and manage packaging components for submissions.
Oversee the Veeva Artwork Process to finalise packaging materials.
Conduct quality reviews using manual and electronic proofreading tools.
Respond to Health Canada queries, including clarifications, screening acceptance, and regulatory extensions.
Maintain accurate project trackers and databases for submission timelines and priorities.
Collaborate with the Canada Regulatory Affairs team on safety-related submissions and updates.
Ensure timely eCTD-compliant submissions in coordination with Regulatory Operations.
🧠 Qualifications & Skills
Graduate or Postgraduate in Pharmaceutical Sciences or a related scientific field.
Minimum 3 years of experience in Regulatory Affairs, specifically in Canadian labelling.
Strong knowledge of Health Canada regulations, XML/SPM development, and regulatory documentation.
Ability to work independently and manage multiple projects with minimal supervision.
Excellent attention to detail and organisational skills.
🌍 Equal Opportunity Commitment
Teva Pharmaceuticals is an equal opportunity employer, committed to fostering a diverse and inclusive workplace. Employment decisions are made without regard to race, gender, age, disability, religion, sexual orientation, or any other legally protected status. If you require accommodations during the recruitment process, Teva will ensure a confidential and accessible experience.
📢 Final Thoughts
This is a fantastic opportunity for professionals looking to grow in the field of regulatory affairs within a globally respected pharmaceutical company. If you have a strong background in Canadian labelling regulations and a passion for ensuring compliance and quality, this role at Teva Pharmaceuticals could be your next career milestone.