Data Solutions Coordinator (Reg Intel) — LATAM
São Paulo, SP, Brazil
- Pay
- Pay not listed
- Work setting
Remote — work setting source
Work setup in the employer’s posting: Remote
From the employer’s posting- Employment
Full-time — employment source
Employment type in the employer’s posting: Full-time
From the employer’s posting
What you’ll work on
Full postingIdentify global regulatory updates and assess their operational and strategic impact
Determine industry scope for regulatory updates
Enter regulatory data accurately into the intelligence platform
Share regulatory intelligence insights and trends with teams and stakeholders
Find and suggest improvements to data processes
From the employer’s posting
Responsibilities include identifying updates, assessing operational and strategic impact, determining industry scope
determining industry scope
ensuring accurate and timely sharing of regulatory intelligence insights
Develops and delivers clear, concise communications across multiple platforms
Seeks opportunities for data process improvement.
What you’ll bring
All qualificationsCore experience
- 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.
Preferred experience
- 4 years' experience in Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence within Pharmaceutical, Biologics, Medical Device, or Animal Health preferred.
Qualification wording
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.
4 years' experience in Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence within Pharmaceutical, Biologics, Medical Device, or Animal Health preferred.
Education & alternatives
- Experience analyzing regulatory updates or compliance-related materials. - A Master’s degree (M.S.) in Regulatory Affairs, Pharmaceutics, or Quality Assurance is preferred. Additional Information
Posting record
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- Live
- First seen by us
- Sep 30, 2026 · 31 days ago
- Recorded sightings
- 23
- Last seen by us
- Oct 31, 2026
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Job description
Job Description
Our 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.
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 an 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.
Additional Information
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.
Company Description
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.
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- Pay
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- Location & working pattern
São Paulo, SP, Brazil
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