Executive Job at Meril | Pharmacovigilance Graduates Apply Now
Meril is hiring an Associate for Global Complaint Management to support its Quality department in Chennai, Tamil Nadu. This Executive Job is ideal for graduates in Science, Medical Engineering, or Pharmacy with 3 to 7 years of experience in complaint handling or regulatory compliance. As an Analyst in the Global Complaints Management team, you will manage the end-to-end lifecycle of device and pharmaceutical complaints, conduct initial triage, and ensure timely regulatory reporting. Join Meril to contribute to global patient safety and work within a world-class, FDA-regulated medical technology environment.
- Job Post: Executive
- Location: Vapi, Gujarat
About The Company
Meril is a global medical device company dedicated to the design and development of innovative, clinically relevant healthcare solutions. Headquartered in India with a strong international presence, Meril specializes in advanced medical technologies across cardiovascular, orthopedic, endo-surgery, and diagnostic segments. Operating in a highly regulated FDA and CE environment, Meril’s Global Complaints Management (GCM) team in Chennai plays a vital role in post-market surveillance, ensuring the highest standards of patient safety and vigilance.
About the Pharmacovigilance Job
- This position will act as a key link between Clinical Operations and Pharmacovigilance, ensuring patient safety, regulatory compliance, and strong vendor/CRO oversight across CGT clinical studies.
Key Responsibilities of the Executive Job
- Oversee outsourced pharmacovigilance vendors and ensure regulatory compliance
- Review and manage SAEs, SUSARs, and ICSR submissions
- Support preparation and review of DSURs / aggregate safety reports
- Collaborate with Clinical, QA, Regulatory, and CRO teams on safety matters
- Provide safety input into protocols, IBs, and clinical documents
- Support inspection readiness, audits, and safety governance meetings
- Manage clinical trial safety activities specific to Cell & Gene Therapy, including long-term safety follow-up
Who Should Apply?
- Background in Pharmacovigilance + Clinical Trials
- Experience in sponsor oversight or CRO/vendor management
- Strong understanding of clinical safety and global PV regulations
- Exposure to Cell & Gene Therapy, Oncology, Rare Diseases, or Advanced Therapies is a plus
- Comfortable working in lean teams and handling cross-functional responsibilities
Why Join the Company
- Opportunity to work on cutting-edge Cell & Gene Therapy programs
- High-impact role with strategic safety oversight, not just operations
- Collaborative, growing sponsor environment
📩 Interested or know someone suitable? Please share the updated resume on – satyaprakash.sharma@microcrispr.com
