Regulatory Affairs Jobs: Teva is Hiring a Regulatory Affairs Associate I | Apply Now for Teva Career
If you looking for pharmacy jobs, specifically regulatory affairs jobs, there is an exciting opportunity in teva career. Teva Pharmaceuticals, a global leader in generic and specialty medicines, is hiring a Regulatory Affairs Associate I in Navi Mumbai. This exciting role offers the opportunity to work in lifecycle management for European and international markets, ensuring regulatory compliance and efficient product management for Teva’s third-party client business, Medis. If you’re a motivated B.Pharm or M.Pharm professional with regulatory experience, this is your chance to build a rewarding career with one of the world’s most trusted pharmaceutical companies.
Job Details:
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Job ID: 64047
About the Company:
Teva Pharmaceuticals is a global leader in generic and specialty medicines, dedicated to improving health and making quality treatments accessible to people around the world. With over 120 years of experience, Teva operates in nearly 60 countries and serves 200 million patients daily with one of the world’s largest portfolios of medicines. The company’s mission is to enhance health and wellness through innovation, reliability, and affordability.
Teva’s commitment to research, development, and manufacturing excellence drives its success in producing medicines that meet the highest quality and regulatory standards. Recognized for its strong global presence and diverse workforce, Teva continues to play a vital role in shaping the future of healthcare.
Education and Experience:
-
Education: B.Pharm / M.Pharm
-
Experience: 1–4 years in Regulatory Affairs with exposure to EU and International markets
Key Responsibilities:
- Manage the lifecycle of assigned products for Europe and international markets.
- Ensure all regulatory modules are updated and compliant with applicable procedures.
- Prepare and submit variations to authorities or Medis clients.
- Track and follow up on submissions, timelines, and approvals.
- Compile and respond to deficiency queries from authorities or clients.
- Maintain up-to-date records, lists, and databases in compliance with procedures.
- Provide regular status updates and performance tracking to management.
- Communicate professionally with internal and external stakeholders.
- Participate in specialized regulatory projects as assigned.
Personal Characteristics:
- Strong organizational and communication skills
- Excellent written and spoken English
- Strategic mindset with adaptability to change
- Team player and proactive problem-solver
- Proficient in computer and documentation systems
Equal Employment Opportunity Commitment
Teva Pharmaceuticals is an equal opportunity employer dedicated to creating an inclusive workplace. Employment decisions are made without regard to age, gender, race, religion, disability, or other protected characteristics. We are committed to providing a diverse and accessible work environment, ensuring every employee can thrive and contribute meaningfully to our shared mission of improving health for all.
