TM Pharmacovigilance

Monitor and analyze adverse drug reactions to uphold patient safety and product efficacy Collaborate with cross-functional teams for regulatory intelligence collection and interpretation Provide expert input to strengthen pharmacovigilance-related customer service Design and implement effective risk management strategies Ensure compliance with global regulatory standards (FDA, EMA, ICH, etc.) Prepare and submit regulatory reports and documentation Conduct in-depth research to refine pharmacovigilance methodologies Facilitate clear communication among internal and external regulatory stakeholders Leverage advanced analytics to improve safety surveillance systems Contribute to drug safety R&D optimization through regulatory insights Integrate regulatory intelligence into company-wide planning and operations Lead continuous improvement initiatives for pharmacovigilance practice Stay updated with industry trends and evolving regulatory frameworks Required Qualifications: B.Pharm or M.Pharm with certifications in: Certified Pharmacovigilance Professional Regulatory Affairs Certification Minimum 25 years of experience in pharmacovigilance and customer service Strong communication skills (verbal and written) in English Ability to adapt to hybrid work setup and rotational shifts Knowledge in regulatory affairs and R&D is preferred Estimated Salary Range: 6 12 LPA (based on experience and certification level) Slug: tm-pharmacovigilance-mumbai-hybrid-rotational-shift .