💊 Teva Pharmaceuticals Hiring – Regulatory Affairs Associate I (Navi Mumbai)
Explore a career in Regulatory Affairs Publishing with Teva Pharmaceuticals, a global leader in generic medicines serving 200M+ patients daily. Join the team in Navi Mumbai and contribute to regulatory submissions for EU, US & Canada markets.
🏢 About Teva Pharmaceuticals
Teva is the world’s leading manufacturer of generic medicines, operating in nearly 60 countries. Committed to making healthcare affordable & accessible, Teva drives innovation, inclusion, and regulatory excellence globally.
📌 Job Details
- Position: Regulatory Affairs Associate I
- Department: Regulatory Affairs (RA Publishing)
- Location: Navi Mumbai, India – 400706
- Experience: 1–3 years (Regulatory Publishing preferred)
- Qualification: B.Pharm / M.Pharm / Master of Life Sciences
- Work Type: On-site
📝 Job Description
Support eCTD publishing & submissions for global markets while ensuring regulatory compliance and quality. Ideal for professionals seeking growth in lifecycle management & regulatory affairs.
Responsibilities:
- Publish & dispatch eCTD submissions for EU, US, Canada 🌍
- Manage post-approval submission publishing & transmission
- Perform document-level publishing and troubleshoot issues
- Conduct quality control checks per agency guidelines ✅
- Collaborate with scientific teams on submission planning & prep
- Maintain knowledge of publishing standards & guidelines
🎯 Skills & Qualifications
- Strong English communication (spoken & written)
- Awareness of cultural diversity in global teams
- Experience with regulatory IT systems: Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, Lorenz Validator
- Basic understanding of ICH, eCTD specs, NeeS, paper submissions
- Experience in EU/US regulatory publishing preferred
- Strong troubleshooting & quality control skills
🎁 Benefits & Perks
- Career growth in a global leader impacting millions
- Inclusive & diverse workplace 🌈
- Learning opportunities in regulatory compliance & IT systems
- Meaningful work contributing to affordable healthcare
- Supportive environment with accessibility accommodations
🚀 How to Apply
Apply via Teva’s official careers portal: https://careers.teva.com/
- Search Job ID 64525 or “Regulatory Affairs Associate I Navi Mumbai”
- Submit your resume & cover letter online
🔗 Verified Job Posting: Teva Career Page
🌟 Why Join Teva?
- Mission-driven culture of innovation & inclusion
- Long-term career stability & global exposure
- Hands-on experience with regulatory processes & IT systems
- Contribute to affordable medicines for millions
❓ FAQs
Q1: What qualifications are required?
A: B.Pharm / M.Pharm / Master’s in Life Sciences with 1–3 years experience; regulatory publishing in EU/US markets preferred.
Q2: How do I apply?
A: Visit Teva Careers → Job ID 64525 → Submit online.
Q3: Is this an on-site role? Which markets does it cover?
A: Yes, on-site in Navi Mumbai. Covers EU, US & Canada submissions.
Q4: What growth opportunities exist?
A: Rapid advancement in regulatory affairs, skill-building in eCTD & IT systems, global exposure, and collaborative learning.
💼 Teva Pharmaceuticals – Your Gateway to Global Pharma Careers!