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Johnson & Johnson

Manager, Case Receipt

Johnson & Johnson

Manager Case Receipt leading operational execution in Global Medical Safety Operations at Johnson & Johnson. Ensuring compliance and quality in case receipt and pharmacovigilance activities.

Posted 7/21/2026full-timeBangalore • 🇮🇳 IndiaSeniorLeadWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in leading operational execution within the pharmaceutical industry, focusing on case receipt activities, regulatory compliance, and process improvement. Proficient in managing team dynamics and performance while ensuring adherence to global safety reporting regulations.

Highest-signal resume keywords
Pharmaceutical Industry ExperiencePharmacovigilance KnowledgeRegulatory Compliance ExpertiseTeam Leadership and DevelopmentProcess Improvement Initiatives

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Case ManagementOperational Metrics DevelopmentKey Performance Indicators MonitoringRisk AssessmentNonconformance ReviewCAPA ActivitiesAudit SupportInspection ReadinessQuality Readiness
Soft Skills
People LeadershipTraining OversightPerformance SupportCollaboration
Tools & Technologies
Pharmacovigilance Safety SystemsArigGlobal LSMVStandard Office Applications
Certifications & Qualifications
RNRPhPharmD
Industry Keywords
Global Case ReceiptDrug SafetyHealth-Related DisciplineScientific DisciplineHigh-Volume Operational Environment

About the role

Key responsibilities & impact
  • Lead daily operational execution and oversight of Global Case Receipt activities
  • Ensure timely, accurate, and compliant execution of case receipt
  • Manage team capacity, resource needs, workload allocation, and staffing priorities
  • Provide people leadership, including training oversight, development planning, and performance support
  • Develop, monitor, and report operational metrics and key performance indicators
  • Partner with internal GMSO functions and other stakeholders to clarify procedures and resolve issues
  • Identify and lead process improvement initiatives and cross-functional projects
  • Support audit, inspection, and quality readiness
  • Lead or support investigations, risk assessments, nonconformance reviews, CAPA activities, and remediation plans

Requirements

What you’ll need
  • Bachelor’s degree in a health‑related or scientific discipline is required
  • Advanced degree (PhD, PharmD) preferred
  • Active professional licensure/certification required for nurses or pharmacists (e.g., RN, RPh, PharmD)
  • Minimum of 8+ years of pharmaceutical industry or clinical experience with a focus on pharmacovigilance and drug safety, including individual case management
  • Demonstrated knowledge of global safety reporting regulations and guidelines and regulatory compliance across the product lifecycle
  • Experience working in a high‑volume, regulated operational environment preferred
  • Proficiency with standard office applications; familiarity with pharmacovigilance safety systems required (ArigGlobal LSMV preferred)

Benefits

Comp & perks
  • Inclusive work environment
  • Diversity and dignity of employees respected