Global Compliance Analyst, TPRM

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic.

Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.

Thrive in the Heart of Europe with QuidelOrtho:

At QuidelOrtho, our Prague office is home to nearly 140 talented professionals supporting critical EMEA Shared Services, including Customer Service, Finance, People & Culture, and GIS. Together, they drive excellence across our global organization.

Our office is ideally located in one of Prague's most attractive districts—just steps from the city center—providing easy access to everything this dynamic city has to offer. Housed in a modern, newly renovated building, the workspace is designed to foster collaboration, flexibility, and well-being—creating an environment where work-life balance truly thrives.

Join us in Prague and become part of a forward-thinking team at the center of it all.

QuidelOrtho is seeking a Global Compliance Analyst, TPRM & Anti-Corruption to join our global team in Prague

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What you'll be doing in your new role:

• Assist with the day-to-day execution of the global Third-Party Intermediary (TPI) Risk Management Program (TPRM), including onboarding, ongoing monitoring, escalation tracking, and offboarding activities.

• Conduct due diligence reviews and assist in applying a risk-based framework tailored to the needs of a global medical device organization operating in complex regulatory environments.

• Assist in ensuring compliance with global Anti-Bribery/Anti-Corruption (ABAC) laws and standards, including the U.S. Foreign Corrupt Practices Act (FCPA), UK Bribery Act, and MedTech Europe Code.

• Assist implementation of risk mitigation activities such as background screening, risk scoring, documentation, and approvals in accordance with internal policies and regulatory expectations.

• Support risk assessments for third parties operating in high-risk jurisdictions, including LATAM, EMEA, and ASPAC, escalate findings as needed.

• Collaborate with Legal, Regulatory, Procurement, and Commercial stakeholders to ensure compliance is integrated into business processes and systems.

• Maintain documentation and tracking tools to support audit readiness and assist with internal audits, inspections, and external regulatory inquiries.

• Assist with process improvement efforts aimed at enhancing program efficiency, transparency, and consistency.

• Contribute to internal and external training initiatives and compliance communication efforts related to ABAC and third-party expectations.

• Monitor and track TPI-related metrics and red flags and assist in preparing summary reports for compliance leadership.

• Collaborate with IT and external compliance service providers to support system enhancements that align with program and user requirements.

• Provide operational support in the development and maintenance of the Compliance Distributor Portal, including uploading resources, managing updates, and tracking usage.

• Contribute to audit remediation efforts by gathering data, drafting process updates, and tracking implementation of corrective actions.

• Prepare customized reports and dashboards with input from compliance leadership, ensuring outputs are clear, actionable and user-friendly.

• Stay informed of regulatory updates, industry best practices, and enforcement developments in FCPA and ABAC.

The individual:

• Minimum Bachelor's Degree, advanced degree a plus.

• Minimum of 3 years of experience in compliance, legal, audit, or risk management, with at least one year in the medical device or life sciences sector preferred.

• Hands-on experience supporting third-party risk management or due diligence programs in a global context.

• Familiarity with FCPA, UK Bribery Act, OECD Guidelines, and ABAC regulatory frameworks.

• Strong organizational and communication skills with an ability to manage competing priorities and deadlines.

What we're offering:

• Competitive salary

• Meal vouchers

• Transportation allowance

• Language courses

• Fit Office

• 3 sick days

• 5 weeks of holidays

• Hybrid-working model

• Employee awards

• Multisport card

• Employee Assistance Program

• Benefit cards and more

The role is based in Prague, Czech Republic.

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