Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Medtronic

Senior Supplier Quality Engineer

Medtronic

. Manage quality oversight of strategic Contract Manufacturers, Original Equipment Manufacturers, and designated suppliers .

Posted 9/21/2026full-timeRemote • United StatesSenior💰 $99,200 - $148,800 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in supplier quality management, including supplier audits, risk assessment, and compliance with regulatory standards. Proficient in leading quality initiatives and collaborating with cross-functional teams to ensure product quality and regulatory adherence in the medical device industry.

Highest-signal resume keywords
Supplier Quality ManagementRegulatory ComplianceNew Product DevelopmentISO 13485 KnowledgeCorrective Action Leadership

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Supplier AuditsRisk AssessmentQuality System RequirementsProcess ValidationTechnical DocumentationSupplier QualificationQuality Standards InterpretationContinuous Improvement InitiativesGMP KnowledgeProduct Acceptance Strategies
Soft Skills
Root Cause AnalysisCross-Functional CollaborationProblem Solving
Industry Keywords
Medical Device IndustryContract ManufacturersOriginal Equipment ManufacturersQuality MetricsSupplier Performance ManagementGlobal Regulatory RequirementsQuality DocumentationSupplier ControlsNonconformance InvestigationProduct Transfer

About the role

Key responsibilities & impact
  • Manage quality oversight of strategic Contract Manufacturers, Original Equipment Manufacturers, and designated suppliers
  • Lead supplier quality activities for product and process changes, including risk assessment, qualification, validation, and implementation support
  • Monitor supplier performance metrics, identify quality risks and trends, and drive corrective and preventive actions
  • Plan, conduct, and support supplier audits for GMP, quality standards, and regulatory compliance
  • Partner with R&D, Regulatory Affairs, Operations, and Quality teams to ensure supplied products and components meet finished device requirements
  • Investigate supplier-related nonconformances, complaints, and quality issues; facilitate root cause analysis and sustainable corrective actions
  • Support New Product Development activities, including supplier qualification, product acceptance strategies, control plans, and supplier quality deliverables
  • Define and maintain receiving inspection requirements, supplier controls, and quality documentation

Requirements

What you’ll need
  • Bachelor’s Degree in Engineering, Science or technical field with 4 years of work experience in Engineering and/or Quality OR Advanced degree in Engineering, Science or technical field with 2 years of work experience in Engineering and/or Quality OR PhD with 0 years relevant experience
  • For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
  • Experience working with supplier quality systems, supplier qualification, supplier audits, or supplier performance management
  • Experience supporting quality processes within a regulated industry environment
  • Experience interpreting and applying quality system requirements, technical documentation, specifications, and quality standards
  • Experience supporting Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), or external manufacturing partners within the medical device industry
  • Experience with New Product Development (NPD), product transfers, process validation, design transfer, or supplier onboarding activities
  • Knowledge of ISO 13485, 21 CFR Part 820, Good Manufacturing Practices (GMP), and global medical device regulatory requirements
  • Experience leading supplier corrective actions, continuous improvement initiatives, and cross-functional quality projects
  • Must possess unrestricted U.S. work authorization at the time of hire and for the duration of employment
  • Travel up to 15% is required

Benefits

Comp & perks
  • Competitive salary and flexible Benefits Package
  • Health, Dental and vision insurance
  • Health Savings Account
  • Healthcare Flexible Spending Account
  • Life insurance
  • Long-term disability leave
  • Dependent daycare spending account
  • Tuition assistance/reimbursement
  • Simple Steps (global well-being program)
  • Incentive plans
  • 401(k) plan plus employer contribution and match
  • Short-term disability
  • Paid time off
  • Paid holidays
  • Employee Stock Purchase Plan
  • Employee Assistance Program
  • Non-qualified Retirement Plan Supplement
  • Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)