Are you passionate about regulatory affairs and data analytics in the life sciences sector? Redica Systems, a leading data analytics startup, is hiring a Data Solutions Coordinator (Regulatory Intelligence) to join their global team in India. This remote, full-time position offers a unique opportunity to work at the intersection of regulatory intelligence and data management, supporting top pharmaceutical and MedTech companies. With a focus on monitoring global regulatory trends, this role is perfect for professionals with 2-4 years of experience in regulatory affairs or quality assurance. Join Redica Systems to make a meaningful impact in a high-growth, tech-forward environment!
About Redica Systems
Redica Systems is a fast-growing data analytics company headquartered in Pleasanton, CA, with a distributed global team. Serving over 200 clients in the life sciences industry, Redica empowers pharmaceutical and MedTech companies to enhance product quality and navigate complex regulatory landscapes. By leveraging proprietary processes and comprehensive datasets from health agencies and FOIA records, Redica provides cutting-edge solutions for inspection preparation, supplier quality monitoring, and regulatory surveillance. Learn more at redica.com.
Responsibilities
As a Data Solutions Coordinator on the Regulatory Intelligence team, you will:
- Monitor Global Regulatory Landscapes: Actively track and categorize regulations, guidelines, and policies in the pharmaceutical and MedTech sectors.
- Analyze Regulatory Data: Utilize GXP knowledge to identify and assess changes in regulations, rules, and guidance documents.
- Ensure Data Integrity: Conduct quality checks to maintain the accuracy and completeness of regulatory data.
- Identify Emerging Trends: Collaborate with cross-functional teams to spot trends in the global regulatory environment.
- Monitor KPIs: Track and report key performance indicators related to regulatory intelligence activities.
- Optimize Processes: Define and improve data acquisition and processing workflows for efficiency and consistency.
Qualifications
To excel in this role, you should have:
- Experience: 2-4 years in the pharmaceutical or medical device industries, with a focus on regulatory affairs or quality assurance.
- Education: A Master’s degree (M.S.) in Regulatory Affairs or Quality Assurance is preferred.
- Skills:
- Effective Communication: Deliver clear, concise updates on regulatory insights to stakeholders.
- Decision-Making: Analyze data to make informed decisions that advance regulatory intelligence goals.
- Organization: Manage multiple time-sensitive projects with high attention to detail.
- Continuous Learning: Stay updated on evolving global regulatory trends.
- Tech Proficiency: Leverage digital tools to monitor and manage regulatory data.
- Engagement: Align with Redica’s values and demonstrate a proactive, collaborative mindset.
Benefits
Redica Systems offers:
- Competitive Salary: A realistic salary range of INR 8,00,000–12,00,000 per year, based on experience.
- Comprehensive Benefits: Health, wellness, and professional development perks.
- Remote Work: Full flexibility to work from anywhere in India.
- Dynamic Team: Collaborate with a global, diverse team in a high-growth startup.
- Career Growth: Opportunities to develop skills in regulatory intelligence and data analytics.
How to Apply
