Regulatory Affairs Job at Teva Pharmaceuticals | Pharma Graduates Can Apply
Teva Pharmaceuticals is hiring for a Regulatory Affairs Job as Regulatory Affairs Associate I (Regulatory Operations – Regulatory Data Analytics) to support its Global Regulatory Affairs (GRA) division. This Regulatory Affairs Job role involves managing regulatory product registration data, ensuring compliance with global standards such as xEVPMD, and maintaining the accuracy of Article 57 data. If you’re passionate about regulatory operations and data analytics in the pharmaceutical industry, this is a perfect opportunity to grow your expertise within a global organization.
Job Position: Regulatory Affairs Associate I
About the Company
Teva Pharmaceuticals is a global leader in generic and specialty medicines, dedicated to enhancing health and expanding access to high-quality treatments worldwide. With a strong focus on innovation, data integrity, and regulatory excellence, Teva empowers patients and healthcare providers by delivering safe and compliant pharmaceutical solutions.
Job Description
The GRO Regulatory Data Analytics role is designed to manage Teva’s regulatory data in compliance with global requirements. This Regulatory Affairs Job ensures:
- Article 57 compliance through accurate management of xEVPMD data.
- Maintenance of Global Regulatory Affairs (GRA) product registration data aligned with Teva’s global standards.
- Subject Matter Expertise (SME) in regulatory data management for current and future systems.
- Execution of data analytics operations to meet the company’s strategic business goals.
Key Responsibilities
- Execute GRO Regulatory Data Analytics operations following established Work Instructions and SOPs.
- Manage product registration data, including data procurement from regulatory dossiers and documentation.
- Demonstrate a strong understanding of regulatory dossier structures, workflows, and registration data management systems relevant to a Regulatory Affairs Job.
- Perform Quality Control (QC) and data integrity checks to ensure accuracy and completeness within Teva’s global registration database.
- Represent GRO Regulatory Data Analytics across the Global Regulatory Affairs community by building effective stakeholder relationships.
- Contribute to business projects that improve regulatory data quality, support system integration, and enhance the regulatory technology landscape.
- Collaborate with cross-functional teams to align data management practices with global compliance standards.
Educational Qualification
B.Pharm or M.Pharm (Pharmacy graduates only).
Experience and Skills
- 1–3 years, preferably in Regulatory Operations or Regulatory Affairs Job roles.
- Proven experience in the pharmaceutical industry with a solid understanding of regulatory processes.
- Experience managing regulatory product registration data within a Regulatory Information Management (RIM) environment is highly preferred.
- Strong understanding of regulatory dossiers, xEVPMD, and Article 57 compliance.
- Excellent analytical and data management abilities.
- Detail-oriented approach with a focus on data accuracy and process compliance.
- Strong communication and interpersonal skills for cross-functional collaboration.
