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Medtronic

Senior Compliance Specialist

Medtronic

. Own and drive investigations, root cause analysis, and resulting corrective and preventive actions .

Posted 10/12/2026full-timeUnited StatesSenior💰 $89,600 - $134,400 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Quality System management, regulatory compliance, and root cause analysis within the healthcare industry. Proficient in implementing FDA, ISO, and GMP standards while effectively communicating and leading quality initiatives.

Highest-signal resume keywords
Quality System ManagementRegulatory Compliance (FDA, ISO 13485, GMP)Root Cause AnalysisData Analysis ToolsLeadership Skills

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills
Quality System ElementsRegulatory RequirementsDesign ControlManufacturing ProcessesTrend AnalysisProblem-Solving TechniquesAudit PreparationCorrective ActionsPreventive ActionsCompliance Observations
Soft Skills
Outstanding Communication SkillsSound JudgementAttention to DetailDecision-MakingProject Management
Tools & Technologies
Data Analysis ToolsQuality Management Systems (QMS)
Industry Keywords
FDA RegulationsISO RequirementsGMPQSRMDSAPHealthcare IndustryRegulatory InspectionsAuditsMedical DevicesCompliance Programs

About the role

Key responsibilities & impact
  • Own and drive investigations, root cause analysis, and resulting corrective and preventive actions
  • Provide Quality System support and guidance to maintain compliance with FDA and international regulatory requirements
  • Oversee development and maintenance of quality systems, programs, processes, and procedures
  • Support EU Surgical Operating Unit entities from a quality oversight perspective, including QMS processes, audits, certifications, production quality issue resolution, PHO, and FCA support
  • Partner with and influence internal and external stakeholders to drive compliance program changes and execution
  • Communicate business-related issues or opportunities to the next management level
  • Lead, coordinate, and/or prepare internal and external audits in accordance with regulatory standards
  • Perform trend analyses and report compliance observations to identify improvement areas
  • Investigate and resolve compliance problems, questions, or complaints from company units, customers, and government regulatory agencies
  • Maintain knowledge of applicable Quality, FDA medical device directives/regulations, HIPAA, and ISO requirements by updating policies and procedures and liaising with policy experts

Requirements

What you’ll need
  • Bachelor’s Degree
  • Minimum of 6 years of relevant experience, or advanced degree with a minimum of 4 years relevant experience
  • Demonstrated knowledge of quality system elements and regulatory requirements, including FDA, GMP, QSR, ISO 13485, and MDSAP, for finished medical devices
  • Ability to implement and communicate quality and regulatory requirements in a government regulated healthcare industry
  • Knowledge of Core QMS, Design Control, and Manufacturing processes/requirements
  • Effective usage of data analysis tools, analytical and research skills, and problem-solving techniques
  • Keen attention to detail and ability to follow an audit trail to identify risks, non-conformances, and true root cause
  • Outstanding written, oral communication, and presentation skills
  • Sound judgement, ability to make decisions, work independently, and demonstrated leadership skills
  • Ability to manage and execute multiple critical projects simultaneously, manage multiple priorities, and escalate issues
  • For Baccalaureate degrees earned outside of the United States, a degree satisfying 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
  • Unrestricted U.S. work authorization at the time of hire and for the duration of employment
  • Approximately 25% domestic and international travel
  • Nice to have: 3 or more years relevant experience in a Design & Development and/or Manufacturing setting
  • Nice to have: Experience supporting or participating in regulatory inspections and audits

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)
  • Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan