Regulatory Affairs Jobs | Teva is Hiring | Apply Now
Looking to start a professional journey in Regulatory Affairs Jobs within the pharmaceutical industry? This Teva Career opportunity for a Regulatory Affairs Associate I is ideal for life science graduates who want to work at the core of global drug regulation and compliance. If you are exploring impactful Life Science Jobs that combine data, documentation, and regulatory strategy, this role offers strong industry exposure and long-term growth.
Job Details
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Job Id: 65585
About the Company
Teva Pharmaceuticals is one of the world’s leading pharmaceutical companies, committed to making quality healthcare more affordable and accessible. Operating in nearly 60 countries, Teva is the world’s largest manufacturer of generic medicines and a major producer of products listed on the WHO Essential Medicines List. Every day, over 200 million people rely on Teva medicines globally. The company is known for its inclusive culture, scientific integrity, and strong focus on regulatory excellence and compliance.
Key Responsibilities
- Responsible for executing GRO Regulatory Data Analytics operations in line with Work Instructions and SOPs. Primarily will be Regulatory Data Analytics Service related to product registration data management (includes the procurement of data from source regulatory documentation which requires a thorough understanding of the structure and contents of a regulatory dossier, and a thorough understanding of the data structures applicable to registration data and the related system workflows).
- Operationally hands-on in terms of carrying out data management activities as an individual contributor. This will require a thorough understanding of the structure and contents of a regulatory dossier (i.e. will be fluent in navigating and understanding the contents of a dossier). Registration data management will require a thorough understanding of the registration data structures, workflows, and applicable work instructions etc.
- Perform Quality Control (QC) and data integrity checking, as part of the Regulatory Data Analytics operation, to confirm the accuracy and completeness of the Teva Global Registration database.
- Represent GRO Regulatory Data Analytics across the wider Global Regulatory Affairs community. Must be proficient at building effective working relationships with all stakeholder and customer groups.
- Responsible for providing effective business project contributions for projects focused on improving regulatory data quality, the provisioning of regulatory data for internal re-use via system integration, or the implementation of any business or technology change that impacts regulatory data or the regulatory technology landscape.
Educational Qualifications
- Required: Bachelor’s or Master’s degree in Life Sciences
- Preferred: MS in a scientific or information technology discipline
Experience
- 1–3 years (preferably with experience in regulatory operations/affairs).
Skills
- Interest in pharmaceutical regulatory affairs. Aptitude for regulatory data management.
- Experience in the pharmaceutical industry with direct involvement in regulatory affairs, demonstrating a strong understanding of the pharmaceutical regulatory process.
- Experience in managing regulatory product registration data, ideally within a regulatory information management environment.
This position is an excellent opportunity for candidates aiming to build a successful Teva Career in regulatory sciences. For life science graduates seeking structured and impactful Life Science Jobs, this Regulatory Affairs Associate I role provides hands-on exposure to global regulatory systems and long-term career advancement in the pharmaceutical industry.
