Teva Hiring: Regulatory Affairs Associate I Position Open for M.Pharm/M.Sc. Graduates in Navi Mumbai

Teva Pharmaceuticals, recognized as a global leader and the world’s largest producer of generic medicines, has announced a significant opening for a Regulatory Affairs Associate I at its Navi Mumbai location. This role is crucial for supporting the company’s regulatory compliance and market access efforts across European and International Markets.

The opportunity targets specialized talent with 2-3 years of industry experience and a Master’s degree, offering a vital entry point into the international compliance framework of a major pharmaceutical firm.

Key Role Functions and Expectations

The successful candidate will operate under the guidance of senior staff, focusing on timely and accurate regulatory execution. Core responsibilities for this role include:

Regulatory Project Management: Driving the completion of assigned projects related to regulatory submissions and maintenance in European and International territories, strictly adhering to internal Work Instructions.
Compliance & Documentation: Rigorously maintaining all regulatory documentation and ensuring data integrity within specialized regulatory IT systems. This includes mandatory proficiency with Veeva Vault and adherence to stringent compliance standards.
Global Communication: Serving as a primary communication conduit with various Teva units across Europe and international regions, third-party partners, and relevant Health Authorities.
Regulatory Intelligence: Staying current with the dynamic landscape of regulatory legislation and guidelines, and ensuring all tasks align with the latest compliance requirements.

Candidate Profile: Qualifications and Core Skills

Teva is searching for well-organized and detail-oriented professionals who possess:

Mandatory Qualification: A Master’s in Pharmacy (M.Pharm) or a Master’s in Science / Life Sciences (M.Sc.) degree.
Experience: A minimum of 2-3 years in the Pharmaceutical Industry. While direct Regulatory Affairs experience is preferred, candidates with strong backgrounds in R&D, Development, or Quality Assurance (QA) will be seriously considered.
Technical Proficiency: Demonstrated working knowledge of Office-365 and, critically, experience with Veeva Vault systems.
Language Advantage: Proficiency in French and/or German will be a notable asset, reflecting the role’s focus on European markets.

How to Apply

Prospective candidates are urged to note the application details:

Job ID: 64000
Location: Navi Mumbai, India
Functional Area: Regulatory Affairs
Application Deadline: October 20, 2025

This position offers a robust platform for professionals seeking to advance their careers in the critical field of pharmaceutical regulatory compliance on a global scale.