Data Solutions Coordinator (Reg Intel) - India

Apitoria Pharma; Bengaluru; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Redica Systems on Bengaluru-based Regulatory Intelligence team monitors global regulatory developments across 150+ countries, combining regulatory science, data structuring, and technology-enabled insights.

The role emphasizes accurate tagging, metadata extraction, and linkage of regulatory documents, with ongoing quality checks to drive actionable intelligence in a fast-paced, high-growth environment.

Qualifications

• 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, with the ability to interpret regulatory language and assess practical industry impact.
• Experience analyzing regulatory updates or compliance-related materials.

Responsibilities

• Monitor regulatory updates across 150+ countries for Pharmaceutical, Biologics, MedTech, and Animal Health sectors.
• Evaluate developments to determine industry scope and operational or strategic impact, distinguishing actionable changes from informational updates.
• Classify and structure regulatory intelligence with metadata extraction, tagging, and linking related documents.
• Maintain awareness of evolving global regulatory frameworks and collaborate to refine monitoring scope and classification logic.
• Ensure data accuracy and integrity through quality checks and KPI monitoring.

Skills

Communicates effectively

Decision making

Data operations

GxP awareness

Regulatory intelligence

Education

Master's degree in Regulatory Affairs/Pharmaceutics/QA

Job description

The Role

Data Solutions Coordinator on the Regulatory Intelligence team at Redica Systems monitors global regulatory developments across 150+ countries. Responsibilities include identifying updates, assessing operational and strategic impact, determining industry scope, and ensuring accurate structured data entry in the regulatory intelligence platform. This role combines regulatory science, data structuring, and technology-enabled intelligence. Strong GxP knowledge, analytical judgment, and attention to detail are essential for this fast-paced, high-growth position.

Key Responsibilities

• Monitor global regulatory authorities (150+ countries) to identify relevant updates impacting Pharmaceutical, Biologics, MedTech, and Animal Health sectors.
• Evaluate regulatory developments to determine industry scope and operational or strategic impact, distinguishing actionable changes from high-volume informational updates.
• Classify and structure regulatory intelligence within the platform, including accurate industry and GxP tagging, metadata extraction (effective dates, consultation deadlines, enforcement timelines), and linkage of related regulatory documents.
• Maintain awareness of evolving global regulatory frameworks, identify emerging trends, and collaborate with internal teams to refine monitoring scope and classification logic.
• Ensure data accuracy and integrity through quality checks, KPI monitoring, and continuous improvement of regulatory intelligence workflows and structured data processes.

About You

• Communicates Effectively: Develops and delivers clear, concise communications across multiple platforms, ensuring accurate and timely sharing of regulatory intelligence insights, updates, and trends with teams and stakeholders.
• Decision Quality: Demonstrates the ability to make good and timely decisions in data operations. Understands the implications of various data choices.
• Optimizes Work Processes: Demonstrates the ability to enhance and streamline data processes. Seeks opportunities for data process improvement.
• Business Insight: Demonstrates the understanding of the business and uses this knowledge to inform data decisions
• Tech Savvy: Demonstrates a basic understanding of current technologies used in data operations. Can effectively use these technologies in daily work and is open to adopting new ones. Qualifications

• 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, with the ability to interpret regulatory language and assess practical industry impact.
• Experience analyzing regulatory updates or compliance-related materials.
• A Master s degree (M.S.) in Regulatory Affairs, Pharmaceutics or Quality Assurance is preferred.

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