MBBS Jobs at Advanz Pharma: Apply Now for Senior Manager Position
MBBS Jobs at Advanz: Advanz Pharma is seeking an experienced and highly skilled Senior Manager – Patient Safety to join its Centre of Excellence in Mumbai. This strategic role is ideal for medical professionals with strong expertise in pharmacovigilance, signal detection, aggregate reporting, and global safety document management. As part of a global pharmaceutical leader in specialty, hospital, and rare disease medicines, this position allows you to drive patient safety excellence across multiple regions and therapeutic categories.
MBBS Jobs at Advanz-Details:
- Position: Senior Manager – Patient Safety
- Location: Andheri (East), Mumbai
About the Company:
Advanz Pharma is a global pharmaceutical company dedicated to improving patients’ lives by supporting the specialty, hospital, and rare disease medicines they rely on. Headquartered in London, the company has a strong international footprint with 700+ employees across 20+ countries—including Europe, Canada, the US, Australia, and India.
MBBS Jobs at Advanz-Qualification:
Education
-
MD / MBBS (mandatory)
Experience & Skills
- Strong experience in Signal Detection
- Hands-on experience with aggregate reporting (PSUR, PADER, etc.)
- Exposure to global pharmacovigilance requirements and guidelines
- Experience handling safety documents across innovator, branded, generic & biosimilar products
- Team handling or leadership experience preferred
- Strong analytical, medical writing, and documentation skills
- Ability to work in fast-paced, multi-regional environments
- Excellent communication and stakeholder management capabilities
Role:
The Senior Manager – Patient Safety oversees global and regional safety document development, signal detection activities, and periodic safety reporting for Advanz Pharma’s full product portfolio. The role ensures compliance with global pharmacovigilance guidelines and maintains high standards in medical safety evaluations, reference safety documents, and risk management activities. This position requires expertise in CCDS/SmPC/PI/PIL writing, safety data interpretation, and end-to-end PV processes for innovator, branded, generic, and biosimilar medicines.
Key Responsibilities:
- Lead creation, update, and medical review of global and regional Reference Safety Documents (RSDs), including CCDS, SmPC, PI, PIL, data sheets, and product monographs.
- Conduct signal detection, validation, analysis, and reporting (including DSR, DEP, SAR as required).
- Draft and medically review PSURs, PADERs, and other aggregate safety reports.
- Perform medical writing for safety assessments, summaries, clinical evaluations, and PV-related documents.
- Contribute to the continuous improvement of PV processes, safety systems, and documentation standards.
- Partner with internal stakeholders, global teams, and external partners to support safety deliverables.
