Navitas Life Sciences is seeking a skilled Safety Associate (RMP) to join its pharmacovigilance and drug safety team in Bangalore (Whitefield). This role is ideal for candidates with 1–4 years of experience in Risk Management Plans (RMP) and Periodic Benefit-Risk Evaluation Reports (PBRER). If you’re passionate about patient safety and regulatory compliance, this is your chance to advance your career in pharmacovigilance.
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🔹 Key Responsibilities
As a Safety Associate (RMP), you will:
- Draft Risk Management Plans (RMP) for innovator products.
- Review and authorize Periodic Benefit-Risk Evaluation Reports (PBRER).
- Support the development and maintenance of RMP documents.
- Collaborate with safety and regulatory teams to ensure compliance with global pharmacovigilance standards.
- Contribute to risk minimization strategies and safety reporting activities.
🎓 Qualifications & Requirements
- Education: M.Pharm, B.Pharm, or Pharm.D
- Experience: 1–4 years in RMP and PBRER-related activities
- Strong knowledge of pharmacovigilance guidelines and regulatory requirements
- Excellent written and verbal communication skills
- Ability to work independently and in cross-functional teams
💼 Job Details
- Position: Safety Associate (RMP)
- Company: Navitas Life Sciences
- Location: Bangalore, Whitefield
- Work Mode: Work from Office / Hybrid
- Employment Type: Full-time
🌟 Benefits of Joining Navitas Life Sciences
- Work in a dynamic and global pharmacovigilance environment
- Exposure to innovator drug safety documentation
- Opportunities for career growth and skill development
- Hybrid working flexibility (based on role requirements)
📩 How to Apply
Interested candidates can apply by sending their updated CV to:
📧 varsha.mane@navitaslifesciences.com
👉 Mention “RMP Role” in the subject line.
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