Data Solutions Coordinator – Reg Intel

🔥 0 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Data Coordinator

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Redica Systems

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2010

🏥 Healthcare

🍽️ Food & Beverage

💼 Consulting

💰 $30M Series B on 2021-12

Healthcare • Food & Beverage • Consulting

Redica Systems is a data analytics platform focused on providing quality and regulatory intelligence for life sciences companies, including those in the pharmaceutical and MedTech sectors. The platform structures unstructured data from various global health agencies and transforms it into actionable insights, which helps companies improve their product quality, manage compliance risks, and enhance regulatory surveillance. Redica Systems' solutions are utilized by over 200 leading firms to address complex GxP compliance challenges, enabling them to move from reactive to proactive strategies.

📋 Description

• Monitor global regulatory authorities across 150+ countries for updates affecting Pharmaceutical, Biologics, MedTech, and Animal Health sectors • Evaluate regulatory developments for industry scope and operational or strategic impact • Distinguish actionable regulatory changes from high-volume informational updates • Classify and structure regulatory intelligence in the platform • Apply industry and GxP tagging • Extract metadata including effective dates, consultation deadlines, and enforcement timelines • Link related regulatory documents • Track evolving global regulatory frameworks and identify emerging trends • Collaborate with internal teams to refine monitoring scope and classification logic • Ensure data accuracy and integrity through quality checks and KPI monitoring • Continuously improve regulatory intelligence workflows and structured data processes • Communicate regulatory intelligence insights, updates, and trends clearly and accurately across platforms

🎯 Requirements

• 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 • Ability to interpret regulatory language and assess practical industry impact • Experience analyzing regulatory updates or compliance-related materials • Master’s degree (M.S.) in Regulatory Affairs, Pharmaceutics or Quality Assurance preferred • Basic understanding of current technologies used in data operations • Ability to effectively use data-operation technologies and adopt new ones

🏖️ Benefits

• Employees can work remotely • Equal opportunity employer • Diverse and inclusive workplace • Confidential handling of applicant information according to EEO guidelines