Regulatory Affairs Specialist II job in Navi Mumbai is a great opportunity for candidates looking to build a stable and high-growth career in the pharmaceutical industry. If you have a background in B.Pharm, M.Pharm, or Life Sciences and are interested in regulatory publishing and global submissions, this role at Teva Pharmaceuticals could be the right step forward.
🌍 About Teva Pharmaceuticals
Teva Pharmaceuticals is one of the world’s leading biopharmaceutical companies, known for its strong generics portfolio and innovative treatments in areas like neuroscience and immunology. The company operates globally and focuses on improving access to high-quality medicines.
Working at Teva offers exposure to international regulatory environments and collaboration with global teams, making it a valuable experience for long-term career growth.
📍 Job Overview
- Position: Regulatory Affairs Specialist II
- Location: Navi Mumbai, Maharashtra
- Job Type: Full-time
- Department: Regulatory Affairs (Publishing)
- Experience Level: Entry to Mid-level
This Regulatory Affairs Specialist II job in Navi Mumbai mainly focuses on eCTD publishing, a critical function in pharmaceutical regulatory submissions.
🧪 Key Responsibilities
In this role, you will handle end-to-end regulatory publishing activities:
- Publish and dispatch eCTD submissions for US, EU, and Canada markets
- Manage lifecycle and post-approval submissions
- Perform document quality checks before submission
- Troubleshoot publishing and formatting issues
- Ensure compliance with ICH, eCTD, and NeeS guidelines
- Collaborate with regulatory and scientific teams
- Work with publishing tools and regulatory systems
This role is ideal for candidates who enjoy structured, detail-oriented work in pharma regulatory operations.
🧠 Required Skills & Qualifications
🎓 Educational Qualification:
- B.Pharm with minimum 2 years of experience, OR
- M.Pharm / Life Sciences Master’s with 0–1 year experience
💡 Technical Skills:
- Knowledge of eCTD publishing
- Understanding of ICH guidelines
- Hands-on experience with tools like:
- Veeva Vault
- Lorenz Validator
- Adobe Acrobat
- ISI Toolbox
- Global Insight
🗣️ Soft Skills:
- Strong written and verbal communication
- Ability to work with global teams
- High attention to detail
- Time management and deadline adherence
🚀 Career Growth in Regulatory Affairs
This Regulatory Affairs Specialist II job offers excellent long-term career potential. Regulatory Affairs is one of the most stable and in-demand domains in pharma.
With experience, you can grow into roles such as:
- Regulatory Affairs Manager
- Submission Publishing Lead
- Global Regulatory Strategist
You will also gain exposure to international markets, which significantly boosts your career value.
💰 Work Culture & Benefits
Teva Pharmaceuticals provides a supportive and growth-oriented work environment:
- Flexible work culture (role dependent)
- Learning & development programs
- Performance-based rewards
- Health and wellness benefits
- Inclusive and diverse workplace
- Internal career mobility opportunities
📊 Who Should Apply?
This Regulatory Affairs job in Navi Mumbai is ideal for:
- B.Pharm candidates with regulatory experience
- M.Pharm freshers looking to enter regulatory affairs
- Candidates interested in eCTD publishing jobs in India
- Professionals seeking stable pharma careers
⚠️ Important Tips Before Applying
- Highlight eCTD publishing experience clearly
- Mention tools like Veeva Vault and Lorenz Validator
- Use ATS-friendly resume format
- Include relevant keywords like:
- Regulatory Affairs
- eCTD
- Submission Publishing
🔗 Apply Now
https://careers.teva/job/Navi-Mumbai-Regulatory-Affairs-Specialist-II-Indi-400706/1377703600
✍️ Final Thoughts
The Regulatory Affairs Specialist II job in Navi Mumbai at Teva Pharmaceuticals is a strong opportunity for candidates aiming to enter or grow in the regulatory domain. With increasing global compliance requirements, skilled professionals in regulatory publishing are in high demand.
If you are detail-oriented, technically skilled, and interested in global pharmaceutical operations, this role is definitely worth applying for.
