PHARMAFull-time
Specialist GxP Product Analysis Pharmacovigilance IT
HYDERABAD (IN)HYBRIDPOSTED: 8/12/2026
PHARMAFull-time
HIRING ORGANIZATIONMSDTechnology
ROLE DEFINITION & RESPONSIBILITIES
Translate PV business needs and regulatory requirements into clear system specifications, user stories, and testable acceptance criteria.
Author, review, and maintain SDLC and validation documentation for GxP-compliant PV software systems.
Collaborate with business stakeholders, IT, validation, and QA teams on system configurations, change controls, and incident resolutions.
Support test planning, User Acceptance Testing (UAT) execution, defect tracking, and release management for PV products.
Ensure documentation and system changes comply with global computer system validation (CSV), GxP standards, and audit requirements.
Work with PV reporting and analytics teams to support dashboard design, data metrics, and system integrations.
REQUIRED VERIFIED SKILLS
Pharmacovigilance
PV Systems
SDLC
GxP Validation
Requirements Management
UAT
Change Control
CSV
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
MSD is actively hiring for this position.
INDUSTRY: Technology
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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