Manager, Regulatory Intelligence (India)

REDICA Systems; United States; Remote; USD 37,000 - 58,000; Full time

Job summary

Redica Systems is seeking a Manager, Regulatory Intelligence to lead a team responsible for monitoring regulatory developments across 150+ countries in life sciences. You will oversee analysis across Pharmaceuticals, Biologics, MedTech, and Animal Health, ensuring data quality and timely delivery within the Regulatory Intelligence platform.

A hands-on leader with strong GxP knowledge and process improvement focus is preferred.

Qualifications

• Regulatory affairs experience in pharma/biotech/medical devices or animal health.
• Experience leading teams with responsibility for quality and delivery.
• GxP knowledge and global regulatory frameworks.
• Experience with regulatory monitoring, data classification, or compliance operations.
• Ability to establish quality standards and improve workflows.
• Comfort with technology-enabled processes and AI/automation tools.
• Master's degree preferred.

Responsibilities

• Lead, coach, and develop a team of Data Solutions Coordinators with clear priorities and performance management.
• Oversee global regulatory monitoring, ensuring timely delivery of developments.
• Guide assessment of regulatory developments, scope, GxP applicability, and impact.
• Maintain standards for structured regulatory data, including metadata and timelines.
• Establish and monitor KPIs for productivity, quality and turnaround.
• Manage workload and priorities to maintain coverage and objectives.
• Collaborate with Product and Engineering to improve monitoring capabilities and workflows.
• Identify opportunities to use AI, automation to improve efficiency and scalability.

Skills

Communicates Effectively

Decision Quality

Optimizes Work Processes

Business Insight

Tech Savvy

Engaged

Education

Master's degree in Regulatory Affairs, Pharmaceutics, Quality Assurance, or related discipline

Job description

Location: India

Redica Systems is looking for a Manager, Regulatory Intelligence to lead a team responsible for monitoring, evaluating, and structuring regulatory developments across 150+ countries.

In this role, you will oversee the quality, accuracy, and timely delivery of regulatory intelligence covering Pharmaceutical, Biologics, MedTech, and Animal Health sectors. You'll guide the team in interpreting regulatory developments, determining industry relevance and impact, and maintaining reliable information within Redica's regulatory intelligence platform.

We're looking for a hands-on leader who brings strong GxP knowledge, sound judgment, and a practical approach to managing people, improving processes, and making effective use of technology.

Key Responsibilities

• Lead, coach, and develop a team of Data Solutions Coordinators, providing clear priorities, guidance, feedback, and performance management.
• Oversee global regulatory monitoring activities, ensuring relevant developments are identified, evaluated, and processed accurately and on time.
• Guide the team's assessment of regulatory developments, including industry scope, GxP applicability, operational impact, and classification decisions.
• Maintain standards for structured regulatory data, including metadata accuracy, effective dates, consultation deadlines, enforcement timelines, and document relationships.
• Establish and monitor team KPIs covering productivity, quality, accuracy, and turnaround times, addressing gaps and improving performance.
• Manage team workload, resource allocation, and priorities to maintain consistent regulatory coverage and meet operational objectives.
• Work with Product, Engineering, and other internal teams to improve monitoring capabilities, classification logic, quality controls, and workflows.
• Identify opportunities to use AI, automation, and other technologies to improve the efficiency, consistency, and scalability of regulatory intelligence operations.

About You

• Communicates Effectively: You develop and deliver clear, concise communications across multiple platforms, ensuring accurate and timely sharing of regulatory intelligence insights, updates, and trends with teams and stakeholders.
• Decision Quality: You demonstrate the ability to make good and timely decisions in data operations. You understand the implications of various data choices.
• Optimizes Work Processes: You demonstrate the ability to enhance and streamline data processes. You seek opportunities for data process improvement.
• Business Insight: You demonstrate an understanding of the business and use this knowledge to inform data decisions.
• Tech Savvy: You demonstrate a basic understanding of current technologies used in data operations. You can effectively use these technologies in daily work and are open to adopting new ones.
• Engaged: You not only share our values but also possess the essential competencies needed to thrive at Redica, as outlined here.

• Familiarity with Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence within Pharmaceutical, Biologics, Medical Device, or Animal Health industries.
• Previous experience leading, supervising, or managing teams, with demonstrated responsibility for work quality, performance, and delivery.
• Strong understanding of GxP principles and global regulatory frameworks, including the ability to interpret regulatory language and assess industry impact.
• Experience overseeing regulatory monitoring, intelligence gathering, data classification, or compliance-related operations.
• Demonstrated ability to establish quality standards, manage operational KPIs, and improve team workflows.
• Comfortable working with technology-enabled processes, data platforms, and AI or automation tools.
• A Master's degree in Regulatory Affairs, Pharmaceutics, Quality Assurance, or a related discipline is preferred.

Top Pharmaceutical Companies, Food Manufacturers, MedTech Companies, and Service Firms from around the globe rely on Redica Systems to mine and process government inspection, enforcement, and registration data. This enables them to quantify risk signals from their suppliers, identify market opportunities, benchmark against peers, and prepare for the latest inspection trends.

Our data and analytics have been cited by major media outlets, including MSNBC, The Wall Street Journal, and The Boston Globe.

Redica Systems is the Intelligence Cloud for life sciences, transforming regulatory complexity into connected, proactive intelligence. Redica's platform helps the world's leading Pharmaceutical and MedTech companies stay inspection-ready, manage supplier risk, and keep pace with evolving global regulations. Built on the Redica Catalyst Platform and powered by Redica ID, Redica unifies the industry's most complete regulatory and inspection datasets, sourced from hundreds of global health authorities, into trusted intelligence for quality and regulatory teams. The Redica Intelligence Cloud brings data together to anticipate risk, accelerate compliance, and enable smarter, faster decisions across the enterprise.

More information is available at redica.com.