Data Solutions Coordinator (Regulatory Intelligence)

Redica Systems

Bengaluru

Presencial

INR 1 500 000 - 2 100 000

Tempo integral

Há 10 dias

Recebe uma resposta deste empregador

O teu currículo e carta de apresentação, adaptados exatamente ao que estão a contratar.

Ultrapassa os filtros ATS

Resumo da oferta

Redica Systems seeks a Data Solutions Coordinator for Regulatory Intelligence to monitor regulatory developments across 150+ countries and transform insights into structured data within our intelligence platform.

Your role blends regulatory science, data structuring, and technology-enabled intelligence, requiring strong GxP knowledge, analytical judgment, and meticulous attention to detail in a fast-growing environment.

Qualificações

  • 3 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 material
  • A Master’s degree (M.S.) in Regulatory Affairs, Pharmaceutics or Quality Assurance is preferred

Responsabilidades

  • 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

Conhecimentos

Communicates effectively
Decision quality
Process optimization
Business insight
Tech savvy

Formação académica

Master's degree (preferred) in Regulatory Affairs/Pharmaceutics/QA

Descrição da oferta de emprego

Redica Systems is a data and analytics SaaS platform that helps regulated industries improve their quality and stay on top of evolving regulations. We are shaping the future of predictive quality with our pioneering work in AI workflows and the development of an exclusive intelligence layer for quality and regulatory data. Our purpose-built processes transform one of the industry’s most complete data sets—aggregated from hundreds of health agencies and unique Freedom of Information Act (FOIA) sourcing—into meaningful answers and insights that reduce regulatory and compliance risk.

Founded in 2010, Redica Systems serves over 200 customers in the Pharma, BioPharma, MedTech, and Food and Cosmetics industries, including 19 of the top 20 Pharma companies and 9 of the 10 top MedTech companies. More information is available at redica.com

The Role

The 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 improvemement
  • 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

  • 3 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 materia
  • A Master’s degree (M.S.) in Regulatory Affairs, Pharmaceutics or Quality Assurance is preferred

Additional information

We are committed to creating a diverse and inclusive workplace where everyone feels welcomed and valued. We believe that diversity of perspectives, backgrounds, and experiences is essential to our success. We are always looking for talented individuals who can bring unique skills and perspectives to our team. All your information will be kept confidential according to EEO guidelines

Obtém a tua avaliação gratuita e confidencial do currículo.

ou arrasta e larga o ficheiro aqui.

Similar jobs

Ofertas semelhantes que vale a pena comparar

Data Solutions Coordinator (Reg Intel) — India
Data Solutions Coordinator (Reg Intel) — India

REDICA Systems • Bengaluru

Presencial
INR 900 000 - 1 300 000
Manager Regulatory Intelligence
Manager Regulatory Intelligence

Redica Systems • Bengaluru

Presencial
INR 2 000 000 - 4 200 000
Data Solutions Coordinator (Reg Intel) - India
Data Solutions Coordinator (Reg Intel) - India

Apitoria Pharma • Bengaluru

Presencial
INR 800 000 - 1 200 000
Manager, Regulatory Intelligence (India)
Manager, Regulatory Intelligence (India)

Apitoria Pharma • Bengaluru

Híbrido
INR 1 800 000 - 3 000 000
Manager, Regulatory Intelligence (India)
Manager, Regulatory Intelligence (India)

REDICA Systems • Bengaluru

Presencial
INR 3 000 000 - 5 000 000
Health insurance
Performance bonuses
Senior Data Engineer
Senior Data Engineer

REDICA Systems • Bengaluru

Presencial
INR 4 000 000 - 5 500 000
Artificial Intelligence Engineer
Artificial Intelligence Engineer

Redica Systems • Bengaluru

Presencial
INR 350 000 - 650 000
AI Engineer
AI Engineer

REDICA Systems • Bengaluru

Presencial
INR 1 500 000 - 3 000 000
Human Resources Partner
Human Resources Partner

Redica Systems • Bengaluru

Presencial
INR 1 800 000 - 2 800 000
Senior RQS Data & Technology Manager
Senior RQS Data & Technology Manager

Merck Healthcare • Bengaluru

Presencial
INR 1 200 000 - 1 600 000