Regulatory Affairs Associate I | B.Pharm/M.Pharm | Teva

Regulatory Affairs Associate I | B.Pharm/M.Pharm | Teva Navi Mumbai

Apply at Teva Pharmaceuticals for Regulatory Affairs Associate I in Navi Mumbai. B.Pharm/M.Pharm with 1–4 years RA experience required.

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Teva Pharmaceuticals, a global leader in generic medicines, is hiring Regulatory Affairs Associate I for its Navi Mumbai office. This role is an exciting opportunity for B.Pharm/M.Pharm graduates with 1–4 years of RA experience to contribute to Teva’s mission of making healthcare more affordable and accessible worldwide.

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Company Overview

Teva Pharmaceuticals is the world’s largest manufacturer of generic medicines, serving more than 200 million people daily across nearly 60 countries. Teva’s portfolio includes many essential medicines listed by the World Health Organization (WHO). With a focus on improving global health, Teva offers employees a collaborative, innovative, and inclusive workplace where they can make a meaningful impact.

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Job Role & Responsibilities

As a Regulatory Affairs Associate I (Product Manager), you will:

• Manage the regulatory lifecycle of assigned Medis dossiers for Teva’s 3rd party client business (Medis).
• Coordinate with Teva’s supply chain, site RA teams, and stakeholders to ensure smooth dossier management.
• Prepare, submit, and follow up on variations to regulatory authorities and Medis clients.
• Compile and submit responses to deficiency letters from authorities or clients.
• Maintain databases, regulatory modules, and records in compliance with procedures.
• Provide regular status updates and reports to management.
• Engage in professional communication with internal and external stakeholders.
• Support audits, inspections, and specialized RA projects as directed.

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Eligibility / Qualifications

• Education: B.Pharm / M.Pharm
• Experience: 1–4 years of experience in Regulatory Affairs with exposure to EU and International markets.
• Skills Required:
  • Strong organizational and documentation skills.
  • Excellent English (written and verbal).
  • Proficiency in MS Office and RA databases.
  • Strategic thinking, adaptability, and proactive approach.
  • Team collaboration and independent work capability.

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Location & Salary

• Location: Navi Mumbai, Maharashtra (PIN: 400706)
• Employment Type: Full-time, Office-based
• Compensation: Competitive salary with global benefits aligned to Teva’s policies.
• Equal Opportunity: Teva is committed to diversity, equity, and inclusion in the workplace.

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Application Process

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

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FAQs

1. What is the required qualification for this role?
B.Pharm or M.Pharm degree with relevant Regulatory Affairs experience.

2. How many years of experience are required?
1–4 years of RA experience with EU/International exposure.

3. What are the main responsibilities?
Lifecycle management of Medis dossiers, handling variations, responding to deficiencies, and ensuring compliance.

4. Where is the job location?
Teva Pharmaceuticals, Navi Mumbai, Maharashtra.

5. Does Teva encourage diversity?
Yes. Teva is an equal opportunity employer promoting a diverse and inclusive workplace.

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Quick Summary Table

Company	Teva Pharmaceuticals
Vacancy	Regulatory Affairs Associate I
Location	Navi Mumbai, Maharashtra (400706)
Required Education	B.Pharm / M.Pharm
Experience	1–4 years in Regulatory Affairs (EU/International markets)
Employment Type	Full-time, Office-based
Salary	Competitive with global benefits
Apply Link	Teva Careers Portal