Safety Reporting Specialist – Thermo Fisher Scientific

A leading global life sciences organization is hiring a Safety Reporting Specialist for a fully remote, full-time role based in Bangalore. This opportunity is ideal for pharmacovigilance professionals with strong expertise in global safety reporting, regulatory compliance, and ICSR submissions.

If you have experience ensuring compliance with international safety regulations, managing regulatory timelines, and mentoring junior team members, this role offers an excellent platform for career advancement in pharmacovigilance and drug safety.

📌 Key Responsibilities – Safety Reporting Specialist

• Receive, prepare, and submit safety reports (ICSRs) to global regulatory authorities
• Ensure all safety reports comply with country legislation and regulatory timelines
• Lead large-scale safety reporting projects and monitor submission performance
• Contribute to the development and improvement of SOPs and procedural documents
• Collaborate with internal departments on safety reporting activities
• Act as a primary point of contact for safety reporting projects
• Mentor and guide new team members and junior colleagues
• Produce safety metrics and support limited financial project activities
• Participate in internal and external meetings related to pharmacovigilance operations

🎓 Qualifications & Experience

• Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline
• Minimum 2+ years of experience in safety reporting or pharmacovigilance
• Strong understanding of global safety reporting requirements
• Excellent knowledge of medical terminology
• Proficiency in Microsoft Office and safety databases
• Strong attention to detail and multi-tasking ability
• Proven skills in problem-solving, critical thinking, and stakeholder communication
• Ability to influence and collaborate across teams

💼 Skills Required

• Global Safety Reporting
• Pharmacovigilance Compliance
• ICSR Submission
• Regulatory Timelines Management
• SOP Development
• Cross-functional Collaboration
• Safety Metrics & Reporting

🎁 Benefits & Work Environment

• Fully remote work model
• Standard Monday–Friday schedule
• Exposure to global pharmacovigilance projects
• Opportunity to work with senior international stakeholders
• Career growth in a regulated, high-impact safety environment

📝 How to Apply

Application Link