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Supplier Risk Management Jobs (NOW HIRING)

Kla

Sr. Manager - Supply Chain Risk

Ann Arbor, MI · On-site

... the supplier risk management framework across direct supply chains, including risk identification, assessment, prioritization, and mitigation. Maintain and govern the supply chain risk register ...

Orbotech

Sr. Manager - Supply Chain Risk

Ann Arbor, MI · On-site

... the supplier risk management framework across direct supply chains, including risk identification, assessment, prioritization, and mitigation. Maintain and govern the supply chain risk register ...

Credit Agricole CIB

$80K/yr

Third Party Risk Management Program is a process of governance to protect the bank from any ... Ensure suppliers that have been on-boarded, have been on-boarded correctly, and that all supplier ...

Visa

Risk Management Analyst

Atlanta, GA · On-site

$89K/yr

Periodically report on supplier risk profiles to various internal business stakeholders. * Triage ... Support Change Management * Drive organizational change initiatives to improve third party risk ...

Exiger

Supply Chain Risk Analyst

Huntsville, AL · On-site

Familiarity with supplier risk, third-party risk, or vendor assessment processes Why Exiger: Exiger is transforming how governments understand and manage supply chain risk. In this role, you will ...

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Supplier Risk Management information

See salary details

$51.5K

$111.6K

$170K

How much do supplier risk management jobs pay per year?

As of Aug 21, 2026, the average yearly pay for supplier risk management in the United States is $111,556.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,000.00 and $129,000.00 per year, depending on experience, location, and employer.

How does a supplier risk management professional typically collaborate with other departments to mitigate supplier-related risks?

Supplier Risk Management professionals work closely with procurement, legal, compliance, and operations teams to identify, assess, and address potential risks in the supply chain. They facilitate regular communication between departments to align on risk thresholds, ensure contract compliance, and implement contingency plans. This collaborative approach helps organizations proactively manage disruptions, maintain regulatory compliance, and safeguard business continuity. Frequent cross-functional meetings and shared risk assessments are common practices in this role.

What are the key skills and qualifications needed to thrive in supplier risk management, and why are they important?

To excel in Supplier Risk Management, you need a strong background in supply chain management, risk assessment, and data analysis, often supported by a business or supply chain degree. Familiarity with risk management software, supplier performance monitoring tools, and relevant certifications such as Certified Supply Chain Professional (CSCP) is highly beneficial. Strong analytical thinking, negotiation skills, and effective communication help professionals build resilient supplier relationships and respond swiftly to potential risks. These competencies are crucial for minimizing disruptions, ensuring compliance, and maintaining the integrity of the supply chain.

What is the difference between Supplier Risk Management vs Procurement Specialist?

AspectSupplier Risk ManagementProcurement Specialist
CredentialsCertifications like CPSM, CSCPCertifications like CPSM, CSCP
Work EnvironmentFocus on risk assessment, supplier evaluationFocus on sourcing, purchasing, vendor negotiations
Industry UsageUsed in supply chain risk mitigationUsed in procurement and purchasing departments
Search IntentCompare risk management roles with procurementCompare procurement roles with risk management

Supplier Risk Management and Procurement Specialist roles overlap in certifications and industry usage, but differ in focus. Supplier Risk Management emphasizes assessing and mitigating supplier risks, while Procurement Specialists concentrate on sourcing and purchasing. Both roles are vital in supply chain operations but serve distinct functions within organizations.

Do supplier risk managers make good money?

Supplier risk managers typically earn a competitive salary that varies by industry, experience, and location. According to industry reports, median salaries range from $70,000 to over $120,000 annually, with additional benefits and bonuses often included. Strong analytical skills and certifications like CPSM can enhance earning potential in this field.

What is supplier risk management?

Supplier risk management is the process of identifying, assessing, and mitigating risks associated with suppliers to ensure supply chain stability. It involves evaluating factors such as financial stability, compliance, and operational performance, often using tools like risk assessments and monitoring systems. Professionals in this field help organizations reduce disruptions and maintain quality standards.
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What cities are hiring for Supplier Risk Management jobs?

Cities with the most Supplier Risk Management job openings:

What states have the most Supplier Risk Management jobs?

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What job categories do people searching Supplier Risk Management jobs look for?

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Supplier Risk Management jobs near you
Infographic showing various Supplier Risk Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $111,556 per year, or $53.6 per hour.

Principal Supplier Quality Engineer

THINK Surgical, Inc.

Fremont, CA • On-site

$165K - $180K/yr

Full-time

Re-posted 15 days ago

Job description

JOB SUMMARY

The Principal Supplier Quality Engineer is the company’s technical leader and subject matter expert for supplier quality management. This position is responsible for developing, implementing, and continuously improving supplier quality systems and supplier performance programs to ensure the consistent delivery of conforming products and services throughout the supply chain.

The Principal Supplier Quality Engineer leads complex supplier quality initiatives, drives supplier quality strategy, mentors quality professionals, and provides leadership in resolving high-risk supplier quality issues. This position plays a critical role in ensuring product quality, patient safety, supply continuity, and regulatory compliance. This position is based in the Fremont, CA office.

DUTIES & RESPONSIBILITIES

  • Lead the development, implementation, and continuous improvement of the company's Supplier Quality Management Program, including supplier management, supplier controls, supplier auditing, supplier monitoring, supplier risk management, and supplier performance processes.
  • Evaluate existing supplier quality systems and implement improvements to harmonize supplier quality practices with FDA QMSR, ISO 13485, ISO 14971, and industry best practices.
  • Manage supplier quality activities throughout the supplier lifecycle, including supplier qualification, monitoring, re-evaluation, development, and disqualification.
  • Lead qualification and oversight of contract manufacturers, sterilization providers, critical suppliers, and other external providers.
  • Plan, conduct, and report supplier audits and supplier assessments to evaluate compliance with quality system, regulatory, and contractual requirements.
  • Establish and maintain supplier quality metrics, supplier scorecards, supplier risk profiles, and supplier performance monitoring programs.
  • Investigate supplier-related quality issues and drive timely resolution through effective root cause analysis, corrective actions, and supplier engagement.
  • Initiate, manage, and close Supplier Corrective Action Requests (SCARs) and monitor supplier effectiveness activities.
  • Evaluate supplier nonconformances and determine appropriate containment, disposition, escalation, and risk mitigation activities.
  • Support incoming inspection activities, supplier issue resolution, supplier change notifications, and supplier process validation activities, as required.
  • Assess the impact of supplier changes on product quality, regulatory compliance, risk management documentation, and product performance.
  • Partner cross-functionally with Engineering, Operations, Manufacturing, Supply Chain, Regulatory Affairs, and externals suppliers to ensure supplier quality requirements are effectively defined, implemented, maintained, and in compliance with FDA Quality Management System Regulation (21 CFR Part 820/QMSR), ISO 13485, ISO 14971, and other applicable regulatory requirements.
  • Support new product development, sustaining engineering, supplier transfer, and supplier qualification activities.
  • Develop and maintain supplier quality procedures, work instructions, forms, templates, and records.
  • Support internal audits, notified body audits, customer audits, FDA inspections, and supplier-related regulatory activities.
  • Support Management Review through supplier quality performance reporting, supplier risk reporting, and quality trend analysis.
  • Provide technical leadership and subject matter expertise for supplier quality, supplier controls, supplier auditing, and supplier risk management activities.
  • Mentor team members and promote adoption of best practices in supplier quality management.
  • Apply risk-based decision making in accordance with ISO 14971 and company procedures.
  • Perform other duties as assigned.

SUPERVISORY RESPONSIBILITIES

  • N/A

QUALIFICATIONS

Required:

  • Bachelor's degree in Engineering, Science, or related discipline, or an equivalent experience.
  • Minimum 8-10 years of Quality Assurance and/or Supplier Quality experience within the medical device industry.
  • Strong working knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, and supplier control requirements.
  • Demonstrated experience qualifying, monitoring, developing, and auditing suppliers.
  • Demonstrated experience managing Supplier Corrective Action Requests (SCARs).
  • Experience conducting investigations, root cause analysis, and corrective action activities.
  • Experience with manufacturing processes, process validation, supplier controls, and quality system requirements.
  • Strong analytical, organizational, and problem-solving skills.
  • Strong written and verbal communication skills.
  • Ability to independently manage multiple priorities and projects.
  • Knowledge of Good Manufacturing Practices (GMP) and applicable Quality System Standards.

Preferred:

  • ASQ Certified Quality Engineer (CQE), Certified Supplier Quality Professional (CSQP), Certified Quality Auditor (CQA), or ISO 13485 Lead Auditor certification.
  • Experience auditing contract manufacturers and critical suppliers.
  • Experience with supplier quality management within medical robotics, orthopedic implants, capital equipment, or electromechanical devices.
  • Experience supporting FDA inspections and notified body audits.
  • Experience with supplier scorecards, KPI development, and quality data analytics.
  • Experience with eQMS systems (e.g., Propel, MasterControl, Arena, etc.).

COMPETENCIES

  • Drive results
  • Decision quality
  • Supplier relationship management
  • Problem solving and root cause analysis
  • Strategic thinking
  • Technical leadership
  • Continuous improvement
  • Attention to detail
  • Risk-based thinking
  • Process improvement
  • Project leadership
  • Effective communication and collaboration
  • Business acumen

PHYSICAL DEMANDS & WORK ENVIRONMENT

  • Must be able to remain in a stationary position and operate office equipment for a prolonged period of time.
  • Physical activities include, but not limited to constant manual dexterity, moving about the work site, and/or handling objects weighing up to 20 lbs.
  • Other infrequent physical activities include, but not limited to, positioning self to complete assigned tasks, and ascending/descending floors and/or ladders.
  • Occasionally work around moving mechanical parts.
  • Must be able to work in a schedule that commensurate with business operation, including work during weekends, holidays and/or times outside of normal business hours.
  • Must be able to travel as business necessitates (up to 50%).

Disclaimer:

The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or physical requirements. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Reasonable accommodations may be possible to enable individuals with disabilities to perform the essential functions.

THINK Surgical, Inc. (“THINK”) is committed to hiring the best qualified candidates for approved positions while engaging in recruitment and selection practices that are in compliance with all applicable employment laws. It is the policy of THINK to provide equal employment opportunity for employment to all applicants and employees, regardless of any protected status. Any qualified applicant or employee with a disability who requires an accommodation in connection with their employment at THINK should contact Human Resources and request an accommodation. THINK also participates in E-Verify, a web-based system that allows THINK to confirm an employee’s eligibility to work in the United States. Actual compensation offered will depend on several factors including but not limited to geographic location, work experience, education, skill level, and/or other business and organizational needs.