Regulatory Affairs Job at Teva Pharmaceutical
Are you looking for a stable and high-growth Regulatory Affairs Job in the pharmaceutical industry? Teva Pharmaceutical Careers brings an excellent opportunity for aspiring professionals to join as a regulatory affairs associate in Navi Mumbai. This is a perfect Job opportunity for life science graduates who want to work in global regulatory submissions, compliance, and pharmaceutical documentation.
About the Company
Teva Pharmaceuticals is a leading innovative biopharmaceutical company supported by a world-class generics business. The organization focuses on advancing treatments in areas such as neuroscience and immunology while delivering high-quality medicines globally. Teva fosters a high-performing and inclusive culture that values innovation, collaboration, and professional growth. Employees are provided with opportunities to balance work and life while contributing to improving global health.
Job Details:
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India – 400706
- Company: Teva Pharmaceuticals
- Job ID: 66406
Role Overview
The Regulatory Affairs Associate I – RA Publishing is responsible for supporting and executing regulatory publishing activities. The role emphasizes maintaining high-quality standards and ensuring timely submissions. The associate serves as a key interface within the regulatory affairs function.
Key Responsibilities
- Publishes and dispatches major and complex routine/lifecycle management eCTD submission projects for EU, US, and Canada markets.
- Handles post-approval submission publishing and ensures high-quality transmission to regulatory agencies.
- Performs document-level publishing activities, including troubleshooting and quality control checks in accordance with agency guidelines.
- Collaborates with scientific teams for planning, preparation, and publishing of submissions.
- Maintains working knowledge of internal and external publishing standards.
- Applies basic knowledge of ICH and eCTD specifications and guidelines (eCTD, NeeS, paper submissions).
- Utilizes technical systems such as Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, and Lorenz Validator.
Qualifications & Experience
- Bachelor’s or Master’s degree in Life Sciences.
- 1–3 years of relevant experience (preferred experience in Regulatory Publishing for EU and US markets).
- Strong command of spoken and written English.
- Awareness and sensitivity to cultural diversity within a global organization.
- Good understanding of regulatory IT systems.
Employee Benefits & Growth
Teva Pharmaceuticals supports employee well-being and career development from day one. Benefits include:
- Generous annual leave and reward programs
- Flexible working arrangements (role-dependent)
- Access to health and wellness support
- Opportunities for community engagement
The company also offers “Twist,” a career development platform providing access to learning programs, short-term projects, and internal growth opportunities. Employees are encouraged to explore and shape their career paths in a supportive environment that prioritizes both professional and personal well-being.
Reporting Structure
Reports to: Manager – Regulatory Submission Management.
