Cencora – Assistant Manager (Pharmacovigilance Quality & Compliance) | Noida, India
Company: Cencora (Affiliated: PharmaLex India Private Limited)
Location: Noida, India
Job Type: Full-Time
Work Mode: On-site / Hybrid (project-based)
Experience: Mid-Level (Pharmacovigilance QA / Compliance)
Qualification: Life Sciences / Pharmacy / Healthcare-related degree
Compensation: Not disclosed in the job description
Pharmacovigilance quality and compliance jobs are rapidly growing, especially roles focused on CAPA management, audit readiness, and PV Quality Management Systems (QMS) in global pharma environments.
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Job Summary
Cencora is hiring an Assistant Manager – Pharmacovigilance Quality & Compliance to lead CAPA management, deviation handling, audit readiness, and PV Quality Management System (QMS) activities. This role is critical in ensuring regulatory compliance, inspection readiness, and continuous quality improvement across pharmacovigilance operations.
You will act as a key point of contact for PV QA and compliance topics, driving root cause analysis (RCA), CAPA effectiveness, and risk mitigation strategies in alignment with global regulatory standards.
This role is ideal for professionals aiming to grow in:
Pharmacovigilance Quality Assurance (PV QA)
Compliance & Audit Management
CAPA & Root Cause Analysis
Regulatory & GxP Quality Systems
Key Responsibilities
CAPA Management & Root Cause Analysis
Perform deviation triage and quality event analysis
Conduct root cause analysis using:
5 Whys
Fishbone (Ishikawa) diagrams
Develop and implement Corrective and Preventive Actions (CAPAs)
Ensure CAPAs include measurable outcomes and effectiveness checks
PV Quality Management System (QMS)
Manage PV QMS controls aligned with:
ICH guidelines
EU GVP
FDA & MHRA regulations
Ensure compliance with client and internal SOPs
Audit & Inspection Readiness
Lead audit coordination (internal and client audits)
Maintain inspection readiness through:
Mock inspections
Evidence documentation
Interview preparation
Support audit findings closure and compliance tracking
Compliance Monitoring & Reporting
Develop and manage PV compliance dashboards tracking:
Right-First-Time (RFT)
ICSR timeliness
CAPA cycle time
Training compliance
Provide data-driven insights to stakeholders
Risk Management & Continuous Improvement
Conduct trend analysis and risk reviews
Drive preventive actions and process improvements
Identify opportunities for automation and workflow optimization
Stakeholder & Client Management
Act as single point of contact for PV QA/Compliance topics
Collaborate with:
Delivery Leads
Medical Safety teams
QA and client stakeholders
Provide clear updates on risks, mitigation plans, and compliance status
Training & Knowledge Sharing
Design and deliver CAPA and compliance training sessions
Facilitate workshops and learning forums for teams
Promote best practices in pharmacovigilance quality
Required Skills & Qualifications
Degree in Life Sciences, Pharmacy, or related field
Experience in:
Pharmacovigilance Quality Assurance (PV QA)
CAPA management and deviation handling
Audit and compliance processes
Strong knowledge of:
ICH-GVP guidelines
Global regulatory frameworks (FDA, MHRA, EU GVP)
Quality Management Systems (QMS)
Expertise in:
Root Cause Analysis (RCA)
CAPA lifecycle management
Strong analytical, communication, and stakeholder management skills
Preferred Skills (High-Impact SEO Keywords):
Pharmacovigilance Compliance
Audit Readiness & Inspection Management
ICSR Timeliness & Quality Metrics
Risk Management & Trend Analysis
SOP Development & GxP Compliance
Quality Dashboards & Data Analytics
Perks & Benefits
Opportunity to work in global pharmacovigilance compliance projects
Exposure to international regulatory audits and QA systems
Career growth in PV quality leadership roles
Collaborative and high-impact work environment
Experience with advanced compliance analytics and dashboards
About the Company
Cencora is a global healthcare solutions provider delivering services across pharmacovigilance, regulatory affairs, and clinical development. Through PharmaLex, the company supports life sciences organizations in maintaining drug safety, compliance, and regulatory excellence.
Why This Role is High-Value in Pharma Careers
The Assistant Manager – PV Quality & Compliance role is essential for maintaining regulatory compliance and inspection readiness in pharmacovigilance operations.
This role provides exposure to:
Global audits and regulatory inspections
CAPA strategy and risk mitigation
Pharmacovigilance quality systems
Data-driven compliance management
Career growth opportunities include:
PV QA Manager
Compliance Lead
Pharmacovigilance Auditor
Quality Systems Head
Application Process
Apply via the official Cencora careers portal
Highlight experience in:
CAPA & Root Cause Analysis
Pharmacovigilance QA
Audit & Compliance
Use keywords:
PV Quality
ICH-GVP
CAPA
Regulatory Compliance
Call to Action
If you want to build expertise in pharmacovigilance quality, compliance, and global regulatory systems, this is your opportunity.
Apply now and become a key driver of quality excellence in drug safety with Cencora 🚀
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