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PHARMA JOBS POST > GOA > Teva Pharmaceuticals Hiring Regulatory Affairs Associate I | Goa Job Opening
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Teva Pharmaceuticals Hiring Regulatory Affairs Associate I | Goa Job Opening

Apply now for the role of Regulatory Affairs Associate I at Teva Pharmaceuticals, Goa. B.Pharm/M.Pharm with 2–4 years of regulatory affairs experience in Europe & International markets preferred. Join the global leader in generic medicines.

ADMIN
Last updated: September 7, 2025 5:43 pm
ADMIN 1 year ago
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Teva Pharmaceuticals, a global leader in generic medicines, is inviting applications for the role of Regulatory Affairs Associate I at its Goa facility. This is a great opportunity for regulatory professionals who want to contribute to making healthcare more affordable and accessible worldwide.

Contents
About Teva PharmaceuticalsJob Opportunity – Regulatory Affairs Associate IKey ResponsibilitiesQualifications & Skills RequiredWhy Join Teva?📍 Location: Goa, India (403722)🆔 Job ID: 63852

About Teva Pharmaceuticals

With operations in nearly 60 countries, Teva is the world’s leading manufacturer of generic medicines and a producer of many products listed on the World Health Organization’s Essential Medicines List. Every day, more than 200 million people around the globe benefit from Teva’s products. The company’s mission is to continuously make a difference in healthcare while offering innovative and affordable treatment options.


Job Opportunity – Regulatory Affairs Associate I

The Regulatory Affairs Associate I will play a vital role in preparing and maintaining the CMC sections (Modules 2.3 and 3) of medicinal product dossiers for international submissions. The position requires close collaboration with cross-functional teams and adherence to regulatory standards across multiple markets.


Key Responsibilities

  • Compile Module 3 and the Quality Overall Summary (Module 2.3) for global submissions.
  • Evaluate dossier content for completeness, accuracy, and regulatory relevance.
  • Assess change controls and prepare regulatory variation packages as per guidelines.
  • Manage CMC queries from regulatory authorities and clients by coordinating with stakeholders.
  • Maintain departmental databases and ensure compliance with SOPs.
  • Collaborate with internal and external teams to support submissions.
  • Stay updated with ICH guidelines, GMP standards, and evolving regulatory requirements (EU, US, and RoW).
  • Ensure accuracy, attention to detail, and compliance with safety and quality standards.

Qualifications & Skills Required

  • Education: B.Pharm / M.Pharm
  • Experience: 2–4 years in Regulatory Affairs, preferably with Europe & International markets.
  • Skills:
    • Strong command of English (written & spoken)
    • Good IT proficiency
    • Excellent communication and organizational skills
    • Ability to work in a team under supervision
    • Result-oriented, proactive, and detail-focused

Why Join Teva?

  • Be part of a global pharmaceutical leader impacting millions of lives daily.
  • Work in an environment that encourages innovation, teamwork, and professional growth.
  • Contribute to affordable healthcare solutions that make a real difference worldwide.

📍 Location: Goa, India (403722)

🆔 Job ID: 63852

If you are passionate about regulatory sciences and aspire to work in a world-class pharmaceutical company, this role at Teva Pharmaceuticals could be the right opportunity for you.

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TAGGED: goa pharma company job, Goa Pharma vacancy, job Opportunity, pharma jobs in goa
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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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