Job Title: TM – Pharmacovigilance
Location: Mumbai Metropolitan Region (Hybrid Work Model)
Job Type: Full-time | Rotational Shifts | No Travel
Job Summary:
We are hiring a TM–Pharmacovigilance professional to oversee and enhance the safety and compliance of pharmaceutical products through adverse event monitoring, regulatory intelligence, and stakeholder collaboration. This hybrid role demands proficiency in English, strong customer service skills within pharmacovigilance, and a commitment to regulatory compliance and process improvement.
Key Responsibilities:
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 2–5 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)
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