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Teva Pharmaceuticals Hiring for Regulatory Affairs

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Teva Pharma

M.Pharm or M.Sc. in Life Sciences, Pharmaceutical Sciences, or related discipline

Navi Mumbai

2–3 years

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Teva Pharmaceuticals, one of the world’s leading manufacturers of generic and specialty medicines, is inviting applications for the role of Regulatory Affairs Associate I in Navi Mumbai, India. This is a golden opportunity for professionals with 2–3 years of experience in post-approval regulatory affairs, especially in EU markets, to contribute to a global mission of making healthcare more affordable and accessible.

If you hold an M.Pharm or M.Sc. degree and are passionate about regulatory compliance, dossier submissions, and maintaining market authorizations, this role at Teva is designed for you.

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🧾 Key Responsibilities

As a Regulatory Affairs Associate I at Teva, your main duties will include:

  • Preparing, compiling, reviewing, and submitting high-quality post-approval regulatory submissions per EU legislation.
  • Ensuring marketing authorization (MA) compliance with legislation and business needs.
  • Monitoring submissions and securing approvals within defined timelines.
  • Maintaining registration documentation and electronic databases.
  • Providing regulatory support and product information to internal teams and stakeholders.
  • Communicating with European agencies and Teva departments across EU regions.
  • Keeping updated on regulatory guidelines, variations, and compliance frameworks.

🎓 Eligibility Criteria & Qualifications

Education:

  • M.Pharm or M.Sc. in Life Sciences, Pharmaceutical Sciences, or related discipline.

Experience:

  • 2–3 years of experience in Post-Approval Regulatory Affairs.
  • Hands-on exposure to European regulatory procedures is desirable.

Skills & Competencies:

  • Excellent oral and written communication.
  • Strong analytical and documentation skills.
  • Knowledge of CTD/eCTD and EU regulatory frameworks.
  • Effective time management, organization, and teamwork abilities.
  • Computer literacy and high attention to detail.

💼 Why Join Teva Pharmaceuticals?

  • Work with a global leader in generic medicine and regulatory innovation.
  • Gain exposure to European market submissions and lifecycle management.
  • Collaborate in a diverse, inclusive, and growth-oriented environment.
  • Opportunities for career advancement and cross-functional learning.

📍 Job Location

Location: Navi Mumbai, Maharashtra, India – 400706
Work Type: Full-time, On-site


💰 Salary Range (Estimated)

INR 5.0 – 7.5 LPA, depending on qualifications and experience.

📝 How to Apply

Application Link

Teva Pharmaceuticals Hiring for Regulatory Affairs
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