Teva Careers: Regulatory Affairs Associate | Apply Now for Chemistry Job
Are you looking for a rewarding chemistry job or exploring growth opportunities within Teva careers? The Regulatory Affairs Associate position in Navi Mumbai is an excellent opportunity for professionals seeking to strengthen their expertise in EU submissions, post-approval processes, and global regulatory operations. This role allows you to contribute to Teva’s mission of making essential medicines accessible worldwide while advancing your career in regulatory affairs.
About the Company
Teva Pharmaceuticals is a global leader in generic medicines and innovative health solutions, offering meaningful career opportunities across regulatory affairs, chemistry, clinical operations, and pharmaceutical development. Joining Teva careers means becoming part of a mission-driven organization that values diversity, scientific excellence, and patient impact. Regulatory roles such as the Regulatory Affairs Associate position allow employees to contribute directly to ensuring safe, compliant, and accessible medicines for millions worldwide.
Job Details
- Job Post: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Job ID: 64984
- Qualification:Â M Pharm or M.Sc.
- Experience: 2 to 3 years in post-approval Regulatory affairs
About the Role
The Regulatory Affairs Associate I role at Teva Pharmaceuticals offers an excellent opportunity for professionals seeking growth in regulatory operations, especially
those transitioning from a chemistry job or pharmaceutical background. In this position, you will support EU post-approval submissions, maintain MA compliance, manage documentation, and collaborate with cross-functional teams across Europe. The role requires strong attention to detail, communication skills, and the ability to meet regulatory timelines. As part of Teva careers, this position provides meaningful exposure to global regulatory processes and contributes directly to ensuring safe, compliant, and accessible medicines for patients worldwide.Responsibilities
- Prepare, compile, review, and submit high-quality submissions for all required post-approval activities in accordance with EU legislation and in-house standards.
- Responsibility for MA compliance with both legislation and business needs.
- Prioritize, plan, and monitor submissions for assigned procedures, documenting and informing involved parties of progress.
- Ensure approvals are secured within the stipulated timelines for designated projects.
- Maintain registration documentation and associated electronic databases, in line with in-house procedures.
- Provide regulatory support and product information for all internal and external customers, stakeholders, and TEVA project teams.
- Communicate with other Teva departments across Europe and European Agencies regarding proposed and pending submissions.
- Maintain and develop awareness of current/pending regulatory legislation and guidelines.
- Fulfilling other allocated department duties and ad-hoc needs at the direction of Senior Regulatory Affairs personnel.
- Awareness of regulatory legislation and guidelines.
Skills
- Desirable to have EU member state experience and knowledge of European regulatory procedures.
- Understanding of processes and departments within a pharmaceutical company.
- Excellent oral and written communication
- Ability to work under pressure and to tight time deadlines
- Effective time and organisation management
- Negotiation
- Initiative
- Analytical (Data and Documentation)
- Computer literacy
- Teamwork and collaboration
- Attention to detail
- Planning and Organisation
