Compliance Expert

6 days ago

Sydney, New South Wales, Australia beBeeCompliance Full time $150,000 - $187,500
Global Compliance Professional

 

Overview

The pharmaceutical and biotechnology sectors are subject to a myriad of laws, regulations, and standards.

Telix does not engage in unsolicited job offers or personal data phishing attempts.

Genuine vacancies are only posted on official channels.

Main Responsibilities
  • Design, develop, and implement a metrics-driven ethics and compliance program.
  • Collaborate with employees to implement a risk-focused compliance program.
  • Lead the development and operationalization of global compliance elements, including monitoring, investigations, policies, and training.
  • Support global implementation of compliance procedures aligned with evolving industry standards and internal risk assessments.
  • Strengthen and lead the company's healthcare compliance investigations process, including intake, tracking, root cause analysis, and corrective actions.
  • Develop and execute risk-based monitoring activities in collaboration with internal audit, quality, and operational functions.
  • Oversee documentation and reporting of findings, escalating critical compliance concerns as needed.
  • Build and manage compliance-related data dashboards and tools to track KPIs, metrics, and trends.
  • Translate insights from investigations and monitoring into actionable recommendations to improve compliance controls and risk mitigation.
  • Contribute to the development of compliance training materials and campaigns to support a culture of integrity and ethical conduct.
Requirements
  • Bachelor's degree in Science, Business, Accounting, Legal, or relevant certifications such as Certified Compliance and Ethics Professional (CCEP).
  • 7+ years' experience working in a legal, compliance, internal audit, or risk management role within the pharmaceutical, biotech, or life sciences industry.
  • Working knowledge of the laws, regulations, and standards that affect companies operating in the radiopharmaceutical, medical device, or biotechnology industries.
  • Strong, proven experience in at least two of the following areas: data monitoring and analysis, risk mitigation, internal audit, systems management, investigations management, and compliance advising.

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