AI-Driven Clinical Risk & Quality Lead

Jobtailor

Woking

On-site

GBP 50,000 - 75,000

Full time

11 days ago
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Job summary

Jobtailor is seeking a Quality & Regulatory Assurance professional in the United Kingdom to manage complaint handling through the lifecycle, support post-market surveillance, and participate in clinical risk management. The role collaborates with Clinical Safety Officers, Product Management, R&D, and Customer Support to address complex safety and product quality issues.

The ideal candidate has 4–7 years of experience in regulated industries, with knowledge of ISO 14971, UK MDR, and EU MDR/IVDR,

Qualifications

  • Bachelor's degree in Life Sciences, Healthcare, Nursing, Biomedical Engineering, Clinical Laboratory Science, Quality, Regulatory Affairs, Information Technology, or a related discipline
  • 4–7 years' experience in Quality, Clinical Safety, Complaint Handling, Post-Market Surveillance, Regulatory Affairs, or Risk Management within a regulated industry
  • Minimum 5 years' experience working with DCB0129 (preferred) and/or DCB0160
  • Experience investigating customer complaints, incidents, adverse events, and product quality issues
  • Experience applying risk management principles in accordance with ISO 14971 or equivalent risk management frameworks
  • Experience with CAPA processes, root cause analysis methodologies, and effectiveness verification activities
  • Working knowledge of UK MDR, EU MDR/IVDR, FDA 21 CFR Part 820/QMSR, and ISO 13485
  • Experience supporting medical devices, diagnostics, healthcare software, laboratory systems, or Software as a Medical Device (SaMD) products
  • Working knowledge of Artificial Intelligence technologies and ability to leverage AI tools in a professional setting
  • Experience with electronic Quality Management Systems (eQMS), complaint management systems, risk management tools, and data analysis platforms
  • Experience using AI-enabled tools for complaint trending, signal detection, and investigation activities
  • Experience with Laboratory Information Systems (LIS) or Laboratory Information Management Systems (LIMS)
  • Knowledge of statistical analysis and trend monitoring methodologies
  • Experience supporting internal audits, external audits, customer assessments, or regulatory inspections
  • Experience across the full product lifecycle, including development, post-market surveillance, complaint handling, and risk management

Responsibilities

  • Manage and support complaint handling activities throughout the complaint lifecycle, including intake, triage, investigation, root cause analysis, corrective actions, and closure
  • Support post-market surveillance through collection, analysis, and interpretation of complaint, service, customer feedback, and product performance data
  • Participate in clinical risk management, including hazard identification, risk assessment, risk evaluation, verification of risk-control effectiveness, and hazard-log maintenance
  • Collaborate with Clinical Safety Officers, Product Management, R&D, and Customer Support teams on complex clinical safety and product quality issues
  • Use AI-enabled tools and data analytics to improve complaint trending, signal detection, root cause analysis, and recurring-issue identification
  • Support compliance with applicable regulatory requirements and improvements in patient safety, product quality, and risk management

Skills

Collaboration
Communication
Problem-Solving

Education

Bachelor's degree in Life Sciences

Tools

eQMS
Complaint Management
Risk Management Tools
Data Analytics
LIS/LIMS
AI Tools

Job description

Jobtailor is seeking a Quality & Regulatory Assurance professional in the United Kingdom to manage complaint handling through the lifecycle, support post-market surveillance, and participate in clinical risk management. The role collaborates with Clinical Safety Officers, Product Management, R&D, and Customer Support to address complex safety and product quality issues.

The ideal candidate has 4–7 years of experience in regulated industries, with knowledge of ISO 14971, UK MDR, and EU MDR/IVDR,

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