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Director Of Risk Control Jobs in Provo, UT (NOW HIRING)

Director of Quality Systems Reports to: CEO Company: Xenter Inc, A TechMed Company About Us Xenter ... Oversee design control processes (DHF, DMR, DHR). * Ensure effective implementation of risk ...

Director of Quality Systems Reports to: CEO Company: Xenter Inc, A TechMed Company About Us Xenter ... Oversee design control processes (DHF, DMR, DHR). * Ensure effective implementation of risk ...

THE ROLE The Director of Quality leads Factory6's Quality and Food Safety organization within a ... control, supplier quality, and risk management. * Provide quality leadership for product hold ...

... of risk mitigation activities by vendors and business owners * Own and manage various actions and task queues that will result from risk management and mitigation activities * Perform quality control ...

... control over safety, compliance, and operations. This is your chance to join a cutting-edge team ... ABOUT THIS ROLE The Director of Hardware Quality leads the end-to-end quality strategy for our ...

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... control over safety, compliance, and operations. This is your chance to join a cutting-edge team ... ABOUT THIS ROLE The Director of Hardware Quality leads the end-to-end quality strategy for our ...

New

... control over safety, compliance, and operations. This is your chance to join a cutting-edge team ... ABOUT THIS ROLE The Director of Hardware Quality leads the end-to-end quality strategy for our ...

... control over safety, compliance, and operations. This is your chance to join a cutting-edge team ... ABOUT THIS ROLE The Director of Hardware Quality leads the end-to-end quality strategy for our ...

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Director Of Risk Control information

See Provo, UT salary details

$10.4K

$134.3K

How much do director of risk control jobs pay per year?

As of May 31, 2026, the average yearly pay for director of risk control in Provo, UT is $133,392.00, according to ZipRecruiter salary data. Most workers in this role earn between $133,400.00 and $133,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director Of Risk Control, and why are they important?

To thrive as a Director Of Risk Control, you need strong expertise in risk management, regulatory compliance, and business operations, often supported by a relevant degree and certifications such as CRM or CPCU. Familiarity with risk assessment software, data analysis tools, and enterprise risk management systems is typically required. Leadership, strategic thinking, and excellent communication skills set outstanding professionals apart in this role. These competencies are critical for effectively identifying, mitigating, and communicating risks to protect organizational assets and ensure regulatory compliance.

How does a Director of Risk Control typically collaborate with other departments to implement effective risk management strategies?

A Director of Risk Control works closely with departments such as operations, legal, compliance, and finance to identify, assess, and mitigate risks across the organization. This role often involves leading cross-functional meetings, developing training programs, and ensuring that risk control policies are integrated into daily business processes. Effective collaboration requires strong communication skills, as the Director must translate complex risk concepts into actionable steps for various teams. Regular reporting and feedback loops help ensure that risk management strategies remain aligned with organizational goals and regulatory requirements.

What does a Director of Risk Control do?

A Director of Risk Control is responsible for developing and implementing strategies to identify, assess, and mitigate potential risks that could impact an organization. They oversee risk management programs, ensure compliance with regulations, and work closely with other departments to promote a safe and secure environment. Their work often involves analyzing data, conducting risk assessments, and providing guidance on best practices to minimize losses or liabilities.

What is the difference between Director Of Risk Control vs Risk Analyst?

AspectDirector Of Risk ControlRisk Analyst
CredentialsBachelor's degree, often advanced certifications (e.g., ARM, CPCU)Bachelor's degree, often certifications like CRM or FRM
Work EnvironmentStrategic planning, leadership, cross-department collaborationData analysis, risk assessment, report preparation
Employer & IndustryInsurance, finance, large corporationsInsurance, finance, consulting firms
Search & Comparison IntentUnderstanding leadership roles in risk managementAnalyzing risk data and assessments

The main difference is that the Director Of Risk Control oversees risk management strategies and leads teams, while a Risk Analyst focuses on analyzing data to identify and assess risks. The director has broader responsibilities and strategic oversight, whereas the analyst is more involved in data-driven risk evaluation.

What job categories do people searching Director Of Risk Control jobs in Provo, UT look for? The top searched job categories for Director Of Risk Control jobs in Provo, UT are:
What cities near Provo, UT are hiring for Director Of Risk Control jobs? Cities near Provo, UT with the most Director Of Risk Control job openings:
Infographic showing various Director Of Risk Control job openings in Provo, UT as of May 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 92% In-person, and 8% Hybrid job distribution, with an average salary of $133,392 per year, or $64.1 per hour.
Director Quality Systems

Director Quality Systems

Xenter

Draper, UT โ€ข On-site

Full-time

Posted 21 days ago


Job description

Location: Draper, UT (In office required)

Job Title: Director of Quality Systems

Reports to: CEO Company: Xenter Inc, A TechMed Company

About Us

Xenter is a technology in medicine company that is bringing medical devices to the digital age. Xenter is revolutionizing medicine by developing and launching smart/wireless guidewires and catheters that transmit data through a proprietary wireless network to our proprietary cloud that collects and houses real-time Physical Intelligence medical data.

Position Summary

The Director of Quality Systems will lead the development, implementation, and continuous improvement of our Quality Management System (QMS). This leader will ensure compliance with:

  • 21 CFR Part 820
  • ISO 13485
  • Applicable FDA and global regulatory requirements

This is a strategic and hands-on leadership role responsible for inspection readiness, scalable quality infrastructure, and cross-functional integration across product development, manufacturing, and post-market activities.

Key Responsibilities

Quality Management System Leadership

  • Build and scale a compliant QMS suitable for a pre-IPO organization.
  • Ensure alignment with FDA Quality System Regulation and ISO 13485.
  • Lead document control, training systems, and record retention programs.
  • Establish quality KPIs and executive-level reporting metrics.

Design Controls & Product Development Support

  • Oversee design control processes (DHF, DMR, DHR).
  • Ensure effective implementation of risk management (ISO 14971 alignment).
  • Partner with Engineering and Regulatory on verification/validation planning.
  • Support software validation and cybersecurity documentation for digital health products.
  • Ensure quality oversight of design changes and product lifecycle management.

CAPA & Post-Market Systems

  • Lead CAPA program, including root cause analysis and effectiveness checks.
  • Oversee complaint handling and MDR evaluation processes.
  • Implement trending and data analytics to drive continuous improvement.
  • Ensure robust post-market surveillance systems are in place.

Supplier & Manufacturing Quality

  • Establish supplier qualification and monitoring processes.
  • Oversee quality agreements and supplier audits.
  • Ensure process validation and production controls are documented and compliant.
  • Support contract manufacturing oversight.

Inspection & Audit Readiness

  • Serve as quality lead during FDA inspections and external audits.
  • Conduct internal audits and manage remediation plans.
  • Prepare executive leadership for agency interactions with the U.S. Food and Drug Administration.
  • Ensure readiness for ISO 13485 certification and surveillance audits.

Qualifications

Required:

  • Bachelorโ€™s degree in engineering, life sciences, or related field.
  • 10+ years of quality systems experience in medical devices.
  • Deep working knowledge of 21 CFR Part 820 and ISO 13485.
  • Experience supporting Class II 510(k) products.
  • Demonstrated experience leading FDA inspections or ISO audits.
  • Strong CAPA and risk management expertise.

Preferred:

  • Experience in a venture-backed or pre-IPO environment.
  • Experience with software-enabled or connected medical devices.
  • ASQ Certified Quality Auditor (CQA) or related certification.
  • Experience implementing eQMS systems.