Regulatory Affairs Jobs at Teva Pharmaceuticals | Life Sciences
Looking for rewarding regulatory affairs jobs in the pharmaceutical industry? Join Teva Pharmaceuticals — a global leader in affordable healthcare solutions. As a Regulatory Affairs Associate I in Navi Mumbai, you’ll play a crucial role in managing regulatory data analytics, ensuring compliance, and supporting the company’s mission to make good health more accessible. This opportunity is ideal for professionals seeking Life Sciences jobs and aiming to build a strong Teva Pharmaceuticals career in global regulatory operations.
- Job Position: Regulatory Affairs Associate I
- Job ID: 61916
- Location: Navi Mumbai, India
About The Company
Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines and a key innovator in affordable healthcare. Operating in nearly 60 countries, Teva’s products appear on the WHO’s Essential Medicines List, serving millions daily. The company’s focus on scientific excellence and global collaboration makes it one of the most trusted names for professionals pursuing a long-term Teva Pharmaceuticals career in Life Sciences jobs and regulatory operations.
At Teva, we are united by one mission — to make quality healthcare more affordable and accessible. With operations in nearly 60 countries, Teva impacts over 200 million people globally every day through its trusted medicines and scientific innovation.
As a Regulatory Affairs Associate I, you will contribute to Teva’s Global Regulatory Operations (GRO) by ensuring high-quality regulatory data analytics and compliance with global standards.
Key Responsibilities
- Execute GRO Regulatory Data Analytics operations in line with SOPs and work instructions.
- Manage product registration data to support regulatory affairs and compliance initiatives.
- Review and extract data from regulatory dossiers with precision and scientific understanding.
- Perform quality control checks and ensure data integrity within Teva’s global registration database.
- Collaborate effectively with internal teams across Global Regulatory Affairs.
- Support projects that enhance regulatory data quality, system integration, and digital transformation within Teva.
Qualifications & Experience
Educational Requirements:
- Bachelor’s or Master’s degree in Life Sciences or Information Technology (mandatory).
- Preferred: Master’s degree in a scientific or IT discipline.
Experience:
- 1–3 years of relevant experience, preferably in regulatory operations or regulatory affairs jobs.
Skills Required:
- Strong interest in pharmaceutical regulatory affairs and data management.
- Knowledge of regulatory dossier structures and data workflows.
- Experience with regulatory information management systems (preferred).
If you’re ready to make a global impact through precision, compliance, and innovation, this Regulatory Affairs Associate I position offers the perfect platform. Apply today to grow with Teva and become part of a dynamic team shaping the future of regulatory affairs jobs and Life Sciences careers in India.
