Regulatory Affairs Associate Job at Teva Pharmaceuticals
Kick-start your regulatory career with teva careers, a global leader in generics and essential medicines. This Associate Job role offers hands-on experience in compiling and maintaining CMC dossiers, collaborating across departments, and contributing to global drug regulatory submissions. Interested candidates in b pharm jobs can apply.
Introduction of the Job
Together, we’re on a mission to make good health more affordable and accessible, helping millions enjoy healthier lives. With operations in nearly 60 countries, Teva is the world’s leading manufacturer of generic medicines and producer of WHO-listed essential medicines. Every day, over 200 million people take our medicines. We continue to explore new ways to make a difference and welcome passionate people to join us. The Associate Job role is responsible for compiling and maintaining the CMC part (modules 2.3 and 3) of medicinal product dossiers for worldwide registrations at TEVA.
Job Details
- Position: Associate Job
- Location: Goa, India – 403722
- Company: Teva Pharmaceuticals
- Experience: 2-4 years (Europe & International RA)
- Education: B.Pharm / M.Pharm
- Job Id: 63852
- Date Posted: Oct 31, 2025
About the Company
Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines, serving 200+ million people globally each day and contributing significantly to global healthcare accessibility. Associate Job Role playa a significant role with the company.
Educational Requirements for Associate Job Role:
- B.Pharm / M.Pharm
- 2-4 years of Regulatory Affairs experience for Europe & International markets
Key Responsibilities for Associate Job Role:
- Compile module 3 and module 2.3 QoS for submission
- Critically evaluate module content for completeness and regulatory compliance
- Assess change controls and prepare variation packages
- Respond to regulatory queries and coordinate with stakeholders
- Maintain departmental databases and tracking systems
- Work closely across departments and business units
- Ensure compliance with ICH, GMP, internal SOPs, and safety requirements
- Stay updated on global regulatory guidelines and industry trends
- Perform additional duties as assigned
Skills Required for Associate Job Role:
- Excellent English communication
- Strong IT and documentation skills
- Team collaboration
- Attention to detail and accuracy
- Responsible, proactive, organized
- Ability to work under supervision
How to Apply for Associate Job Role:
Interested candidates in b pharm jobs can apply and Visit teva careers website for application details and submission alerts.
