Teva Pharmaceuticals, a globally recognized biopharmaceutical leader with a strong generics and specialty portfolio, is inviting applications for the position of Regulatory Affairs Associate I at its Navi Mumbai location. This opportunity is ideal for professionals with experience in regulatory operations, regulatory compliance, data management, and pharmaceutical regulatory affairs reporting.
If you are looking to build a career in Global Regulatory Affairs (GRA), especially within EU Gx metrics and compliance reporting, this role offers strong exposure to international regulatory systems and cross-functional collaboration.
🔎 Job Overview – Regulatory Affairs Associate I
The Regulatory Affairs Associate I will support Global Regulatory Affairs Compliance by managing regulatory metrics, reporting, and data retrieval from internal RA systems. The role involves working closely with R&D, portfolio management, and regulatory teams to ensure regulatory data integrity and compliance.
This position focuses heavily on:
- EU Gx & Specialties regulatory metrics
- Regulatory database management
- GRIDS data entry and retrieval
- Global regulatory reporting
- SOP & Work Instruction lifecycle management
📌 Key Responsibilities
- Prepare and maintain EU Gx metrics and regulatory compliance reports
- Generate global and regional ad-hoc regulatory reports
- Perform GRIDS data entry and data analysis
- Retrieve and analyze data from Teva RA systems
- Support Global Regulatory Affairs (GRA) compliance initiatives
- Assist in SOP management via DMS & LMS systems
- Monitor periodic review cycles for regulatory documentation
- Liaise with cross-functional teams (R&D, Portfolio, Regulatory Affairs)
- Ensure regulatory data accuracy, completeness, and compliance
🎓 Qualifications & Eligibility Criteria
Required:
- Bachelor’s or Master’s degree in Life Sciences or Information Technology
- 1–3 years experience in:
- Regulatory Operations
- Regulatory Affairs
- Pharmaceutical / Biotechnology / Medical Device Industry
- Strong experience in:
- Data management
- Handling large regulatory datasets
- Database systems & data retrieval
Preferred:
- MS in Scientific or IT discipline
- Exposure to regulatory reporting systems
💼 Preferred Skills for Regulatory Affairs Associate Role
- Knowledge of EU Gx regulatory reporting
- Familiarity with regulatory databases (GRIDS, RA systems)
- Experience in SOP lifecycle management
- Analytical skills for compliance metrics
- Strong attention to regulatory detail
- Proficiency in IT tools and reporting systems
💰 Salary (Estimated Range)
Based on market standards in Navi Mumbai for 1–3 years Regulatory Affairs professionals:
₹5,50,000 – ₹8,00,000 per annum (CTC)
(Final salary may vary based on experience and internal structure.)
🌟 Benefits at Teva Pharmaceuticals
- Competitive compensation & reward plans
- Flexible working schedule (role-dependent)
- Health & wellbeing support programs
- Career development platform (Twist)
- Internal mobility opportunities
- Inclusive and diverse work culture
Teva promotes equal employment opportunities and provides accommodation support during recruitment.
📍 Job Location
Navi Mumbai, Maharashtra – 400706, India
India