Data Solutions Coordinator – Reg Intel

Redica Systems

. Monitor global regulatory authorities across 150+ countries for updates affecting Pharmaceutical, Biologics, MedTech, and Animal Health sectors .

Posted 9/29/2026full-timeRemote • IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Regulatory Affairs and GxP principles, with a strong ability to analyze and communicate regulatory intelligence insights across the Pharmaceutical, Biologics, MedTech, and Animal Health sectors. Proficient in data operations and ensuring data accuracy and integrity through quality checks.

Highest-signal resume keywords

Regulatory Affairs ExperienceGxP Principles UnderstandingRegulatory Intelligence AnalysisData Operation Technologies ProficiencyMaster's Degree in Regulatory Affairs

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Regulatory IntelligenceRegulatory AnalysisGxP ComplianceData Accuracy MonitoringMetadata ExtractionRegulatory Document LinkingQuality AssuranceRegulatory Framework EvaluationActionable Regulatory Change IdentificationRegulatory Language Interpretation

Soft Skills

CollaborationCommunicationAnalytical ThinkingAttention to DetailContinuous Improvement

Tools & Technologies

Data Operation TechnologiesRegulatory Intelligence Platforms

Industry Keywords

PharmaceuticalBiologicsMedTechAnimal HealthGlobal Regulatory FrameworksRegulatory UpdatesCompliance MaterialsKPI MonitoringConsultation DeadlinesEnforcement Timelines

About the role

Key responsibilities & impact

Monitor global regulatory authorities across 150+ countries for updates affecting Pharmaceutical, Biologics, MedTech, and Animal Health sectors
Evaluate regulatory developments for industry scope and operational or strategic impact
Distinguish actionable regulatory changes from high-volume informational updates
Classify and structure regulatory intelligence in the platform
Apply industry and GxP tagging
Extract metadata including effective dates, consultation deadlines, and enforcement timelines
Link related regulatory documents
Track evolving global regulatory frameworks and identify emerging trends
Collaborate with internal teams to refine monitoring scope and classification logic
Ensure data accuracy and integrity through quality checks and KPI monitoring
Continuously improve regulatory intelligence workflows and structured data processes
Communicate regulatory intelligence insights, updates, and trends clearly and accurately across platforms

Requirements

What you’ll need

4 years' experience in Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence within Pharmaceutical, Biologics, Medical Device, or Animal Health preferred
Strong understanding of GxP principles and global regulatory frameworks
Ability to interpret regulatory language and assess practical industry impact
Experience analyzing regulatory updates or compliance-related materials
Master’s degree (M.S.) in Regulatory Affairs, Pharmaceutics or Quality Assurance preferred
Basic understanding of current technologies used in data operations
Ability to effectively use data-operation technologies and adopt new ones

Benefits

Comp & perks

Employees can work remotely
Equal opportunity employer
Diverse and inclusive workplace
Confidential handling of applicant information according to EEO guidelines