Regulatory Affairs Associate I Jobs at Teva Pharmaceuticals Navi Mumbai with eCTD publishing exposure and global regulatory career growth
About the Company
Teva Pharmaceuticals is a global pharmaceutical leader committed to making good health more affordable and accessible. With operations in nearly 60 countries, Teva is the world’s leading manufacturer of generic medicines and a major producer of products listed on the World Health Organization’s Essential Medicines List. Every day, more than 200 million people worldwide rely on Teva medicines, making a meaningful difference in global healthcare. Regulatory Affairs Associate I Jobs
At Teva, diversity, inclusion, and innovation come together to support patients, communities, and employees across the globe. Regulatory Affairs Associate I Jobs at Teva Pharmaceuticals
Job Details
- Job Title: Regulatory Affairs Associate I (RA Publishing)
- Job ID: 64525
- Location: Navi Mumbai, Maharashtra, India – 400706
- Employment Type: Full Time
- Experience Required: 1–3 Years
- Department: Regulatory Submission Management
- Reports To: Manager – Regulatory Submission Management
Job Description
Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I to support Regulatory Publishing activities for global markets. This role focuses on high-quality, on-time electronic regulatory submissions, primarily for the EU, US, and Canada. The position offers excellent exposure to lifecycle management submissions, post-approval activities, and regulatory IT systems within a global pharmaceutical environment. Regulatory Affairs Associate I Jobs
Key Responsibilities
- Publish and dispatch major, complex, and routine eCTD lifecycle management submissions for EU, US, and Canada markets
- Handle post-approval regulatory submissions and ensure timely transmission to health authorities
- Perform document-level publishing activities in compliance with agency requirements
- Conduct quality control checks on submission-ready documents as per regulatory guidelines
- Troubleshoot document and publishing-related issues effectively
- Collaborate with scientific and regulatory teams for planning, preparation, and publishing activities
- Maintain compliance with internal and external publishing standards
- Apply basic knowledge of ICH guidelines and regulatory submission formats including eCTD, NeeS, and paper submissions
- Ensure 100% quality and adherence to submission timelines
Regulatory Affairs Associate I Jobs at Teva Pharmaceuticals
Skills / Qualifications
Educational Qualification
- B.Pharm / M.Pharm / Master’s degree in Life Sciences
Experience
- 1–3 years of total experience preferred
- Prior experience in Regulatory Publishing for EU and US markets is an advantage
Technical Skills
- Working knowledge of regulatory publishing tools and systems such as:
- Global Insight
- Veeva Vault
- ISI Toolbox
- Adobe Acrobat
- Lorenz Validator
- Understanding of regulatory IT systems and submission workflows
Soft Skills
- Strong command of written and spoken English
- High attention to detail and quality
- Ability to work in a global, culturally diverse organization
- Good communication and collaboration skills
Regulatory Affairs Associate I Jobs
Benefits / Perks
- Opportunity to work with a global pharmaceutical leader
- Exposure to international regulatory submissions (EU, US, Canada)
- Inclusive and diverse work culture
- Professional development and learning opportunities
- Stable and growth-oriented regulatory career path
Regulatory Affairs Associate I Jobs at Teva Pharmaceuticals
Why You Should Join
- Be part of a mission-driven organization improving global access to healthcare
- Gain hands-on experience in global regulatory publishing and eCTD submissions
- Work in a collaborative, multicultural environment
- Build a strong foundation for long-term growth in Regulatory Affairs
- Contribute directly to high-quality regulatory submissions impacting patient access worldwide
Regulatory Affairs Associate I Jobs at Teva Pharmaceuticals
How to Apply
FAQs
Is this role suitable for early-career professionals?
Yes, candidates with 1–3 years of experience in Regulatory Affairs or Publishing are encouraged to apply.
Which markets will I work on?
You will primarily support regulatory submissions for the EU, US, and Canada.
Is regulatory publishing experience mandatory?
It is preferred but not mandatory. Candidates with strong regulatory knowledge and IT system exposure will be considered.
What submission formats will I work with?
eCTD, NeeS, and paper-based submissions as per agency requirements.
Does Teva support workplace diversity and inclusion?
Yes, Teva is committed to equal employment opportunity and maintaining a diverse, inclusive workplace.
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