Medicine Job: Senior Medical Reviewer Role at Lupin in Mumbai
A promising medicine job opportunity is available at Lupin Limited for the role of Senior Manager DSRM (Medical Reviewer) in Mumbai. This position offers experienced professionals the chance to contribute to pharmacovigilance, signal detection, and safety review activities while working with a leading pharmaceutical organization. Candidates looking for medical jobs in Mumbai and exploring Lupin careers can find an exciting career path through this role.
Job Details:
- Job Title: Senior Manager DSRM (Medical Reviewer)
- Location: Airoli, MH, IN
About the Company
Lupin Limited is a globally recognized pharmaceutical company known for developing and manufacturing high-quality medicines across multiple therapeutic areas. With a strong presence in pharmacovigilance and drug safety, Lupin careers offer professionals the opportunity to contribute to innovative healthcare solutions while working in a collaborative and research-driven environment.
Job Description
This medicine job at Lupin Limited involves oversight and management of Medical Review and Signal Management related activities. The role focuses on medical review of safety reports, signal detection, evaluation activities, and pharmacovigilance documentation. Professionals working in medical jobs in Mumbai within this role will contribute to safety monitoring, literature review, and support pharmacovigilance processes as part of expanding Lupin careers in drug safety.
Qualifications
- Doctorate, Graduation in Medicine
- Work Experience: 5 to 10 years of Pharmacovigilance experience with preferred expertise in aggregate report, signal detection, clinical safety/SAE management.
Key Responsibilities
- Oversight and management of Medical Review and Signal Management related activities
- Medical Review of Health Hazard Assessment and Knowledge sharing and training of DSRM team as required
- Signal detection and evaluation activities and Aggregate reports
- Medical review and approval of Individual Case Safety Reports and Providing inputs for MR Post Procedure Quality Check (PPQC)
- Review of relevant literature articles for aggregate reports and signal activities
- Supporting team in preparing device malfunction report and drafting response for Health Authority request
- Review of Quality investigation reports and Review and approval of case deletion form
- Review of any pharmacovigilance documents after relevant training as required and Provide inputs for SOPs and other guidance documents preparation
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