Pharma Regulatory Affairs Associate Job at Teva Pharmaceuticals | Apply Now
Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I in Navi Mumbai, India. This role offers an exciting opportunity to contribute to one of the world’s leading pharmaceutical companies, ensuring regulatory compliance and supporting approvals for essential medicines. With a strong foundation in post-approval regulatory affairs and EU procedures, candidates can play a pivotal role in making healthcare more affordable and accessible to millions worldwide.
- Job Posting: Regulatory Affairs Associate I
- Location: Navi Mumbai
- Company: Teva Pharmaceuticals
- Job Id: 63835
About Teva Pharmaceuticals
Teva Pharmaceuticals is one of the world’s leading pharmaceutical companies, specializing in the development, production, and distribution of generic medicines, specialty medicines, and innovative treatments. With operations in nearly 60 countries, Teva provides high-quality healthcare solutions to over 200 million people every day. The company is dedicated to improving access to affordable medicines while maintaining a strong focus on innovation, patient well-being, and global health.
Qualification
Desirable Experience
- 2–3 years of experience in post-approval regulatory affairs.
- Overall 2–3 years of experience in the pharmaceutical industry.
- EU regulatory knowledge and experience preferred.
Job Requirements
- Prepare, compile, review, and submit high-quality submissions for post-approval activities in line with EU legislation.
- Maintain marketing authorization (MA) compliance with regulations and business requirements.
- Prioritize, plan, and monitor submissions while updating stakeholders on progress.
- Communicate with European agencies and other Teva departments on regulatory matters.
- Maintain awareness of current and pending regulatory legislation and guidelines.
Why Apply Here
This role provides the chance to work with the world’s leading manufacturer of generic medicines and be part of a mission-driven organization impacting millions globally. As a Regulatory Affairs Associate at Teva, you will contribute to ensuring compliance and timely approvals that directly support patient health. The role also offers exposure to international regulatory procedures, professional growth opportunities, and the chance to be part of a diverse, global team.
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