Manager, Regulatory Intelligence

🔥 0 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

👻 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.

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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

• Lead, coach, and develop a team of Data Solutions Coordinators • Provide clear priorities, guidance, feedback, and performance management • Oversee global regulatory monitoring activities across 150+ countries • Ensure relevant regulatory developments are identified, evaluated, and processed accurately and on time • Guide 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 • Address performance gaps and improve team performance • Manage team workload, resource allocation, and priorities • 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

🎯 Requirements

• 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 • Clear, concise communication across multiple platforms • Ability to make good and timely decisions in data operations • Ability to enhance and streamline data processes • Understanding of business context to inform data decisions • Basic understanding of current technologies used in data operations and openness to adopting new technologies • Ability to lead, supervise, or manage teams

🏖️ Benefits

• Employees can work remotely