Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.
Post : Regulatory Affairs Associate - RIMS
Inviting applications for multiple roles in our RA Team for Regulatory Information Management role.
Experience : 1-10 years
Qualification : Bachelor's Degree in Life Sciences or Information Technology or MS in scientific or information technology discipline
• Experience of the pharmaceutical industry with direct experience in Regulatory Affairs managing regulatory product registration data.
• Excellent understanding of the regulatory requirements of Article 57 (2) of Regulation (EC) No 726/2004 (Extended EudraVigilance Medicinal Product Dictionary or xRVMPD) and the related record submissions process.
Job Location : Navi Mumbai
Candidate must have experience into XEVMPD.
Interested suitable applicants are requested to share their updated CV on pranita.padte@teva.co.in with the subject line as RA-RIMS role.
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