Home Regulatory Affairs Regulatory Affairs Associate | Teva Pharmaceuticals | Navi Mumbai, MH

Regulatory Affairs Associate | Teva Pharmaceuticals | Navi Mumbai, MH

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Teva is a global pharmaceutical leader and the world’s largest generic medicines producer committed to improving health and increasing access to quality Health solutions worldwide.

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Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development, and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Position: Regulatory Affairs Associate I

Location: Navi Mumbai, Maharashtra

Job Description:

  • Prepare, compile, review, and submit high-quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards.
  • Responsibility for MA compliance with both legislation and business needs.
  • Ensure approvals are secured within the stipulated timelines for designated projects.
  • Maintain registration documentation and associated electronic databases, in line with in-house procedures.
  • Provide regulatory support and product information for all internal and external customers, stakeholders, and TEVA project teams.
  • Prioritize, plan, and monitor submissions for allocated procedures while documenting and informing involved parties of progress.
  • Communicate with other Teva departments across Europe and European Agencies regarding proposed and pending submissions.
  • Maintain and develop an awareness of current/pending regulatory legislation and guidelines.
  • Fulfilling other allocated department duties and ad-hoc needs at the direction of Senior Regulatory Affairs personnel.

Qualification: B.Pharma/M.Pharma/M.Sc

Experience: 3-4 Years Relevant Experience, Post Education in EU Market

Salary: Negotiable

Contact Details:

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