Teva Pharmaceuticals Hiring Regulatory Affairs Associate
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Teva Pharmaceuticals?
- FAQs
- Summary Table
Regulatory Affairs Associate I – Teva Pharmaceuticals, Navi Mumbai
Apply for Regulatory Affairs Associate I at Teva Pharmaceuticals, Navi Mumbai. 1–3 years experience in EU market required.
Teva Pharmaceuticals, a leading global pharmaceutical company, is inviting qualified professionals to join as Regulatory Affairs Associate I for the EU market at its Navi Mumbai office. This role offers a prime opportunity to work in regulatory operations, product registrations, and compliance with EU regulations in a dynamic, growth-oriented environment.
Company Overview
Teva Pharmaceuticals is a globally recognized pharmaceutical and biotechnology company committed to delivering high-quality medicines and healthcare solutions. With a strong presence in over 60 countries, Teva focuses on innovation, regulatory compliance, and patient-centric solutions. The company’s Navi Mumbai facility plays a pivotal role in supporting EU regulatory submissions, ensuring adherence to international standards and contributing to global healthcare advancement.
Job Role & Responsibilities
Position: Regulatory Affairs Associate I – EU Market
Location: Navi Mumbai
Key Responsibilities:
- Manage regulatory product registration data and submissions for the EU market.
- Work within a Regulatory Information Management System (RIMS) environment.
- Ensure compliance with EU regulatory guidelines and requirements.
- Coordinate with cross-functional teams including Quality, Manufacturing, and Regulatory departments.
- Track deadlines, maintain records, and support dossier preparation and submission.
- Respond to regulatory queries and maintain regulatory documentation integrity.
Eligibility / Qualifications
Educational Qualification:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, Biotechnology, or related fields.
Experience Required:
- 1–3 years in regulatory operations or regulatory affairs.
- Experience managing EU market regulatory submissions and working with RIMS systems.
Important Notes:
- Freshers are not eligible.
- Only candidates with EU regulatory experience will be considered.
Location & Salary
Work Location: Navi Mumbai, Maharashtra
Employment Type: Full-Time
Salary: Competitive, based on experience and industry standards.
Teva offers a collaborative work environment with exposure to global regulatory frameworks, career development opportunities, and employee benefits aligned with industry best practices.
Application Process
Interested and eligible candidates are encouraged to send their updated CV to:
Apeksha.Shinde01@teva.co.in
Apply before 20 October 2025 to secure your consideration.
Documents to Include:
- Updated Resume
- Academic Certificates
- Experience Certificates
Why Join Teva Pharmaceuticals?
- Work in a global pharmaceutical leader with a strong reputation in generics and branded medicines.
- Gain experience in EU regulatory frameworks and product registration processes.
- Collaborate with experienced professionals in a structured and regulated environment.
- Opportunities for career growth, skill enhancement, and exposure to international standards.
FAQs
1. Who is eligible for this position?
Candidates with 1–3 years of experience in Regulatory Affairs or Operations specifically for the EU market with a Bachelor’s or Master’s degree in Life Sciences or Pharmacy.
2. Can freshers apply?
No, this role requires prior experience in EU regulatory affairs.
3. What are the primary responsibilities?
Managing regulatory product registration data, coordinating EU submissions, and maintaining compliance with regulatory guidelines.
4. What is the job location?
Navi Mumbai, Maharashtra.
5. How can candidates apply?
Send your updated CV to Apeksha.Shinde01@teva.co.in before the deadline.
Summary Table
| Category | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Vacancies | Regulatory Affairs Associate I – EU Market |
| Required Education | Bachelor’s or Master’s in Life Sciences, Pharmacy, Biotechnology, Pharmaceutical Sciences |
| Experience | 1–3 Years in EU regulatory affairs |
| Location | Navi Mumbai, Maharashtra |
| Application Email | Apeksha.Shinde01@teva.co.in |
| Last Date to Apply | 20 October 2025 |
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