Teva Pharmaceuticals is seeking a highly motivated and experienced Regulatory Affairs Associate I to join their team in Navi Mumbai. As a key member of the regulatory affairs team, you will play a critical role in managing regulatory product registration data and supporting regulatory operations.
📍About the Role
Job Title: Regulatory Affairs Associate I
Location: Navi Mumbai
Experience: 1-3 years in regulatory operations or affairs
Job Type: Full-time
🧩Responsibilities
Regulatory Data Management: Manage regulatory product registration data in a regulatory information management system (RIMS) environment.
Regulatory Operations: Support regulatory operations, including tracking and maintaining regulatory documents and submissions.
Collaboration: Work closely with cross-functional teams, including regulatory affairs, to ensure seamless delivery of regulatory projects.
Data Analysis: Analyse and interpret regulatory data to support business decisions.
🎓Requirements
Education: Bachelor’s or Master’s degree in Life Sciences or Pharmacy.
Experience: 1-3 years of experience in regulatory operations or affairs, with experience managing regulatory product registration data in a RIMS environment.
Skills:
Strong understanding of regulatory requirements and guidelines.
Proficiency in regulatory information management systems (RIMS).
Excellent written and verbal communication skills.
Ability to work independently and prioritise tasks effectively.
🌟What We Offer
Career Growth: Opportunities for professional growth and development within a leading pharmaceutical company.
Collaborative Environment: Dynamic and supportive team environment that encourages innovation and creativity.
Competitive Benefits: Attractive salary and benefits package.
📧 Interested candidates can send their updated CV to
👉 Apeksha.Shinde01@teva.co.in