Pharma Regulatory Affairs Jobs at Teva | M Pharm Candidates Apply Now
Are you looking for a rewarding career in Regulatory Affairs? Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I in Navi Mumbai, offering the chance to work with the world’s leading manufacturer of generic medicines. This role focuses on lifecycle management for Medis dossiers, regulatory submissions, and stakeholder collaboration, making it an excellent opportunity for pharmacy graduates with EU and international market experience.
About the Company
Teva Pharmaceuticals is a global leader in generic and specialty medicines, dedicated to improving health and increasing access to affordable treatments for patients around the world. Headquartered in Israel, Teva operates in nearly 60 countries and supplies medicines to approximately 200 million people every day. Our broad portfolio includes generics, specialty medicines, and biopharmaceutical products across diverse therapeutic areas. With more than a century of expertise, Teva combines innovation, scientific excellence, and a commitment to quality to transform healthcare and make a meaningful difference in people’s lives. We are proud to be the world’s leading manufacturer of generic medicines and a trusted partner in global healthcare.
Job Detail
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Job ID: 64047
- Qualification: B Pharm / M Pharm
- Experience: 1–4 years of relevant Regulatory Affairs experience with EU & International markets
The Opportunity
The Regulatory Affairs Associate I acts as a Product Manager (PM) responsible for RA lifecycle management of Medis dossiers within Teva’s third-party client business. This includes ensuring information flow, documentation support, and close collaboration with Teva’s supply chain, site RA, and other key functions.
How You’ll Spend Your Day:
- Manage lifecycle activities for specific products across Europe and international markets
- Keep regulatory modules up to date in accordance with procedures
- Prepare, inform, and submit variations directly to authorities or to Teva’s Medis client business
- Track variation submissions, timelines, and approvals
- Compile answers to deficiency questions from authorities or clients
- Communicate outcomes of variations promptly and maintain accurate databases/lists
- Provide regular status updates to management
- Participate in goal setting and follow-ups with supervisors
- Maintain professional communication with internal and external stakeholders
- Work on specialized RA projects as assigned
Personal Characteristics:
- Strong organizational skills
- Effective communication and presentation abilities
- Excellent written and verbal English
- Strategic thinker with adaptability to change
- Team-oriented with a proactive and independent work approach
- Good computer proficiency
Keywords: Pharma Regulatory Affairs Associate job, Navi Mumbai, Teva Pharmaceuticals careers India, RA jobs for B Pharm, M Pharm, Regulatory lifecycle management roles in pharma.
