Regulatory Affairs Job Vacancy at Teva Pharmaceuticals | MSc Life Science Graduates Apply Now
Looking to build a career in regulatory affairs with one of the world’s leading pharmaceutical companies? Teva Pharmaceuticals is hiring a Regulatory Affairs Associate I in Navi Mumbai, India (Job ID: 63620). This role is ideal for candidates with a Master’s in Pharmacy or Life Sciences and 2–3 years of experience in post-approval regulatory affairs. Join Teva and contribute to making healthcare more affordable and accessible for millions worldwide.
- Job Position: Regulatory Affairs Associate I
- Location: Navi Mumbai, Maharashtra, India – 400706
- Job ID:63620
About the Company
Teva Pharmaceuticals is a global leader in generic medicines and a producer of many products listed on the World Health Organization’s Essential Medicines List. With a presence in nearly 60 countries and drugs used by over 200 million people every day, Teva is committed to improving global healthcare accessibility. Working at Teva means being part of a diverse team that is shaping the future of medicine.
Job Description
As a Regulatory Affairs Associate I at Teva, you will play a critical role in supporting regulatory submissions, ensuring compliance with EU regulations, and maintaining product approvals. This position requires expertise in regulatory processes
, attention to detail, and the ability to work with cross-functional teams to meet strict timelines.Key Responsibilities
- Prepare, compile, review, and submit high-quality submissions for post-approval activities in line with EU legislation and company standards.
- Ensure compliance with Marketing Authorization (MA) requirements, including legal and business obligations.
- Plan, prioritize, and monitor submissions while keeping all stakeholders informed of progress.
- Secure regulatory approvals within stipulated timelines for assigned projects.
- Maintain registration documentation and electronic databases.
- Provide regulatory support and product information to internal and external stakeholders.
- Communicate with European agencies and other Teva departments regarding regulatory submissions.
- Stay updated on current and upcoming regulatory guidelines and legislation.
Qualifications
- Education: Master’s degree in Pharmacy, Science, or Life Sciences.
- Experience: 2–3 years in post-approval regulatory affairs within the pharmaceutical industry.
Preferred Skills:
-
- Knowledge of European regulatory procedures.
- Strong communication and negotiation skills.
- Ability to manage time effectively under tight deadlines.
- Excellent analytical and organizational skills.
- Proficiency with regulatory databases and documentation systems.
- Team-oriented with high attention to detail.
Keywords: Teva Pharmaceuticals, Regulatory Affairs Associate, Navi Mumbai, EU Procedures, Regulatory Affairs Job Vacancy, Pharmaceutical Industry, Equal Employment Opportunity, Jobs
