Teva Pharmaceuticals Hiring for Regulatory Affairs Associate (1-3 Years Exp)

Explore Regulatory Affairs Associate I jobs at Teva Pharmaceuticals in Navi Mumbai. Join pharma jobs in regulatory publishing for EU, US, and Canada markets, advancing pharmaceutical careers in India with global impact.

About the Company

Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines, operating in nearly 60 countries with a diverse workforce. Committed to making good health affordable and accessible, Teva serves over 200 million people daily through innovative products on the WHO Essential Medicines List.

The company fosters a culture of inclusion, regulatory excellence, and continuous growth, driving impactful healthcare solutions worldwide.

Job Details

• Company Name: Teva Pharmaceuticals
• Experience: 1-3 years (preferred in Regulatory Publishing for EU and US markets)
• Qualification: B.Pharm / M.Pharm / Master of Life Sciences
• Location: Navi Mumbai, India, 400706
• Work Type: On-site

Job Description

Teva Pharmaceuticals is seeking a Regulatory Affairs Associate I to support publishing and dispatching regulatory submissions, ensuring compliance and quality in global markets. This role interfaces with regulatory teams to manage eCTD projects, ideal for entry-level professionals in pharmaceutical careers in India focused on lifecycle management.

Regulatory Affairs Associate I

• Department: Regulatory Affairs (RA Publishing)
• Market: EU, US, Canada
• Role: Publish and ensure quality of routine/lifecycle eCTD submissions
• Experience: 1-3 years
• Education/Qualification: B.Pharm / M.Pharm / Master of Life Sciences

Skills/Qualifications

• Proficiency in spoken and written English
• Sensitivity to cultural diversity in a global organization
• Good understanding of regulatory IT systems like Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, Lorenz Validator
• Basic knowledge of ICH, eCTD specifications, NeeS, and paper submissions
• Preferred experience in regulatory publishing for EU and US markets
• Strong troubleshooting and quality control skills for documents

Key Responsibilities

• Publish and dispatch eCTD submissions for EU, US, Canada
• Handle post-approval submission publishing and transmission
• Perform document-level publishing and troubleshoot issues
• Conduct quality control checks per agency guidance
• Collaborate with scientific teams on planning and preparation
• Maintain knowledge of publishing standards and guidelines

Benefits/Perks

• Career growth in a global leader serving 200 million daily
• Inclusive, diverse workplace with equal opportunity commitment
• Opportunities for learning in regulatory compliance and IT systems
• Impactful role in affordable healthcare innovation
• Supportive environment with accommodations for accessibility

How to Apply

To apply for this Regulatory Affairs Associate I position, visit Teva’s official careers portal at https://careers.teva.com/ and search for Job ID 64525 or “Regulatory Affairs Associate I Navi Mumbai.” Submit your resume and cover letter online.

Verified Post

Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Teva Career page.

For more pharma jobs, check Pharma Recruiter. Teva values diversity—apply today and contribute to global health accessibility!

Why You Should Join

Teva Pharmaceuticals champions a mission-driven culture of innovation and inclusion, recognized for equal employment opportunities across its global operations. Employees gain long-term career stability through exposure to cutting-edge regulatory processes and diverse teams.

Thrive in an environment blending compliance expertise with collaborative growth, making a tangible difference in affordable medicines for millions worldwide.

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