Regulatory Affairs Associate Job At Teva Pharmaceuticals
Jumpstart your career in Regulatory Affairs with Teva Pharmaceuticals. The company is hiring for a Regulatory Affairs Job to assist with FDA submissions, annual reports, and change control documentation, providing hands-on experience in a global pharmaceutical environment. Graduates seeking M Pharma jobs or Pharma jobs can apply now.
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, Maharashtra, India – 400706
About the Company
Teva Pharmaceuticals is a leading global manufacturer of generic medicines and a trusted producer of essential medicines listed by the WHO. Teva serves over 200 million patients daily and is committed to making healthcare affordable and accessible worldwide.
Key Responsibilities
- Prepare FDA annual reports, supplements, and amendments under supervision
- Review supporting documents for change controls, ensuring compliance and accuracy
- Maintain regulatory databases and trackers in real-time
- Familiarize with FDA regulations and guidance to support filings
- Perform other regulatory and documentation duties as assigned
Educational Requirements
- M. Pharma in Regulatory Affairs/QA is preferred
- Relevant experience in analytical/QC, R&D/laboratory, or production in pharma/biotech
Skills Required
- Knowledge of FDA regulations and submission processes
- Basic computer skills (Word, Excel, Internet)
- Strong organizational, detail-oriented, and multitasking abilities
- Good verbal and written communication
- Ability to work independently and in teams
Why This Job Role?
This Regulatory Affairs Job role provides a strong foundation in regulatory affairs within a global pharmaceutical environment, offering exposure to FDA submissions, change control processes, and hands-on experience in regulatory compliance. Graduates seeking M Pharma jobs or Pharma jobs can apply now.
