Regulatory Affairs Job Vacancy at Teva Pharmaceuticals | MPharm 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 daily, Teva is committed to enhancing 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:
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- 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
