Regulatory Affairs Associate I – Teva Pharma Hiring

Regulatory Affairs Associate I – Teva Pharma Hiring, Navi Mumbai

Apply for Regulatory Affairs Associate I at Teva Pharmaceuticals, Navi Mumbai. B.Pharm/M.Pharm/Life Sciences graduates with 1–3 years experience preferred.

Teva Pharmaceuticals, the world’s leading manufacturer of generic medicines, is seeking a Regulatory Affairs Associate I for its Navi Mumbai facility. This full-time role offers an exciting opportunity to contribute to global regulatory publishing activities, ensuring timely, accurate, and compliant submissions for EU, US, and Canadian markets. If you are a pharmacy or life sciences graduate with regulatory publishing experience, this role could be your gateway to a rewarding career in regulatory affairs.

Company Overview

Teva Pharmaceuticals is on a mission to make good health more affordable and accessible. Operating in nearly 60 countries, Teva supplies medicines to 200 million people worldwide every day. The company is a proud producer of many products listed on the World Health Organization’s Essential Medicines List. With a rich heritage in generics, innovative specialty medicines, and biosimilars, Teva combines global expertise with local insights to improve healthcare worldwide.

Joining Teva means being part of a diverse team, committed to delivering excellence, innovation, and patient access to essential therapies.

Job Role & Responsibilities

As a Regulatory Affairs Associate I – RA Publishing, you will:

• Publish and dispatch complex lifecycle management eCTD submissions for EU, US, and Canada.
• Manage post-approval submission publishing and ensure timely, quality submissions to regulatory agencies.
• Perform document-level publishing activities, troubleshoot issues, and conduct quality control checks.
• Collaborate with scientific personnel for planning, preparation, and publishing submissions.
• Maintain up-to-date knowledge of internal/external publishing standards and regulatory guidelines.
• Work with technical systems such as Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, and Lorenz Validator.
• Apply knowledge of ICH and eCTD specifications/guidelines for regulatory compliance.

Eligibility / Qualifications

• Education: B.Pharm, M.Pharm, or Master’s in Life Sciences.
• Experience: 1–3 years (regulatory publishing experience in EU/US markets preferred).
• Skills:
  • Strong command over written and spoken English.
  • Familiarity with regulatory IT systems.
  • Sensitivity to global cultural diversity.

Relevant courses under eligibility: B.Pharm, M.Pharm (Pharmaceutics, Pharmaceutical Analysis, Regulatory Affairs), M.Sc Biotechnology, M.Sc Life Sciences, M.Sc Biochemistry, M.Sc Microbiology.

Location & Salary

• Location: Navi Mumbai, Maharashtra, India – 400706
• Work Model: Full-time, onsite
• Compensation: Competitive salary based on experience, with industry-standard benefits
• Reporting To: Manager – Regulatory Submission Management

Application Process

Interested candidates can apply directly via Teva’s official career portal:
Apply Here

Why Join Teva Pharmaceuticals?

• Contribute to a company that **serves 200+ mil