Regulatory Affairs Associate I Job At Teva Pharmaceuticals
Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I in Navi Mumbai for professionals interested in regulatory publishing and global submissions. This Regulatory Affairs Job role offers hands-on exposure to EU, US, and Canada regulatory environments while working with one of the world’s largest generic pharmaceutical companies. Graduates seeking B pharma jobs or M Pharma jobs can apply now.
Job Details
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India (400706)
About the Company
Teva Pharmaceuticals is one of the world’s leading manufacturers of generic medicines, operating across nearly 60 countries. Teva products are listed on the World Health Organization’s Essential Medicines List and are used daily by more than 200 million people worldwide. Teva’s mission is to make good health more affordable and accessible globally.
Educational Requirements for Regulatory Affairs Job
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Bachelor of Pharmacy (B.Pharm)
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Master of Pharmacy (M.Pharm)
Key Responsibilities
Regulatory Publishing & Submissions
- Publish and dispatch major, complex, and routine lifecycle eCTD submissions for EU, US, and Canada markets.
- Handle post-approval regulatory submissions and ensure high-quality submission delivery to agencies.
- Perform document-level publishing activities and troubleshoot publishing issues.
Quality Control & Compliance
- Conducting quality control checks on submission-ready documents as per agency guidelines is required for Regulatory Affairs Job role.
- Maintain compliance with internal and external publishing standards.
- Ensure adherence to ICH and eCTD specifications, including eCTD, NeeS, and paper submissions.
Collaboration & Systems Management
- Collaborate with scientific and regulatory personnel for planning, preparation, and publishing activities.
- Maintain working knowledge of regulatory IT systems and tools such as Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, and Lorenz Validator.
Skills Required for Regulatory Affairs Job
- Strong understanding of regulatory publishing processes
- Knowledge of ICH guidelines and eCTD specifications
- Experience with regulatory IT systems and publishing tools
- Excellent spoken and written English communication skills
- Attention to detail and strong quality orientation
- Ability to work effectively in a global, culturally diverse environment
Why This Job Role?
This Regulatory Affairs Job role offers exposure to global regulatory submissions, hands-on experience with eCTD publishing, and the opportunity to work with international teams. It is ideal for professionals looking to build a strong career in regulatory affairs within a globally recognized pharmaceutical organization. Graduates seeking B pharma jobs or M Pharma jobs can apply now.
