Regulatory Affairs Jobs at Teva Pharmaceuticals Careers – Navi Mumbai | Apply Now
Regulatory Affairs Jobs at Teva Pharmaceuticals Careers present an excellent opportunity for regulatory professionals seeking growth in a global biopharmaceutical organization. This Regulatory Affairs Associate I role in Navi Mumbai focuses on FDA submissions, annual reports, and regulatory compliance, making it an ideal opening for candidates aiming to build a strong career in Regulatory Affairs Jobs with Teva Pharmaceuticals Careers.
Job Details
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Job ID: 65573
About the Company
Teva Pharmaceuticals Careers represent opportunities within a leading innovative biopharmaceutical company supported by a world-class generics business. Teva works across neuroscience, immunology, and high-quality medicine delivery worldwide. Employees joining through Teva Pharmaceuticals Careers become part of a high-performing, inclusive culture that values collaboration, innovation, flexibility, and professional growth while contributing to better global health.
Job Description
Under direct supervision, the Regulatory Affairs Associate I prepares regulatory submissions such as supplements, amendments to supplements, and annual reports in accordance with FDA guidelines. As part of Regulatory Affairs Jobs at Teva Pharmaceuticals Careers, the Associate I assists in evaluating change controls to ensure accuracy of submitted documents. Annual Report submission and all associated responsibilities are the primary responsibility of this position. The role also includes maintaining regulatory databases and trackers in real time.
Key Responsibilities
- Prepare annual reports under direct supervision and assist with FDA supplements as experience is gained
- Review documents supporting change controls, including batch records, methods, and specifications
- Familiarize with FDA regulations and guidance used in filing determinations
- Maintain approved applications in compliance with FDA regulations for assigned ANDA Annual Reports
- Populate and maintain regulatory and team databases and trackers accurately
- Perform additional duties and projects as assigned
Qualifications
- M Pharma degree in the RA/QA discipline is a plus
- Minimum of two years Regulatory Affairs experience and/or analytical, QC, R&D, laboratory, or production experience in the pharmaceutical or biotech industry
- Basic computer skills, including Word, Excel, and internet usage
- Ability to work independently and in team environments
- Good verbal and written communication skills
- Strong organizational skills with attention to detail and multitasking ability
Employee Benefits
Teva Pharmaceuticals Careers offers comprehensive benefits from day one, including generous annual leave, reward plans, flexible working schedules (role-dependent), tailored health support, and opportunities to give back to the community. Teva also supports career development through its Twist platform, providing learning programs, short-term projects, and internal growth opportunities while prioritizing employee well-being.
