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Global drug and device development services

Risk & Compliance Lead

Regulatory Compliance & EthicsPosted on Nov 11
Full-time

About the Job

Requirements

  • Relevant experience within Pharmacovigilance, Drug Safety, Quality, Compliance, or another regulated pharmaceutical or clinical research environment.
  • A good understanding of regulated operational processes and associated quality and compliance requirements.
  • Experience working with quality metrics, deviations, Corrective and Preventive Actions, audit findings, and Root Cause Analysis.
  • Exposure to audits, inspections, compliance reviews, or inspection-readiness activities.
  • Strong analytical and problem-solving skills, with the ability to identify trends, outliers, and areas of potential risk.
  • The ability to work collaboratively with operational teams to investigate issues and develop practical, sustainable solutions.
  • Strong communication and stakeholder management skills, with the confidence to raise and escalate risks appropriately.
  • The ability to manage competing priorities and follow actions through to resolution.
  • A proactive approach to continuous improvement, quality, and compliance.
  • Employment requires the legal right to work in the country where the role is based.

Responsibilities

  • Monitor agreed quality and compliance metrics, identify risks, trends, and outliers, and escalate potential non-compliance or areas requiring further action.
  • Provide focused review and analysis of metrics for specific clients or projects when required.
  • Support operational teams with the management of Quality Events, including deviations, Corrective and Preventive Actions, and audit findings.
  • Support investigations and Root Cause Analysis, helping to identify underlying causes and appropriate corrective and preventive actions.
  • Assist operational teams with audit and inspection readiness, including preparation for and support during client audits and regulatory inspections.
  • Support the effective management and resolution of audit and inspection findings, working collaboratively with relevant stakeholders.
  • Contribute to system and process optimisation initiatives, using quality data and operational insight to identify opportunities for improvement.
  • Work cross-functionally to promote risk awareness and a culture of quality, compliance, and continuous improvement.

Desired Qualifications

  • A bachelor's degree in life sciences, pharmacy, healthcare, law, business, quality, risk management, or a related field.
  • A professional certification in quality, risk management, or compliance.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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