Supplier Quality Manager

Johnson & Johnson

. Establish and monitor robust quality assurance programs for external manufacturers .

Posted 9/24/2026full-timeUnited StatesMid-LevelSenior💰 $102,000 - $177,100 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in establishing and monitoring quality assurance programs, supplier quality systems, and regulatory compliance within the medical devices and pharmaceutical industries. Proven ability to lead cross-functional teams, drive continuous improvement initiatives, and manage risk effectively.

Highest-signal resume keywords

Quality Assurance ProgramsSupplier Quality SystemsRegulatory ComplianceRisk ManagementSix Sigma/Process Excellence

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Quality MetricsNonconformance ManagementCAPAChange ManagementManufacturing Process Controls

Soft Skills

LeadershipCommunicationProblem SolvingNegotiationJudgement

Certifications & Qualifications

Six Sigma Certification

Industry Keywords

Medical DevicesPharmaceutical IndustryGMPSupply ChainR&D

About the role

Key responsibilities & impact

Establish and monitor robust quality assurance programs for external manufacturers
Oversee supplier quality systems, manufacturing process controls, product quality performance, risk management and regulatory compliance
Lead Source Quality and Purchasing Controls for external manufacturers
Drive supplier qualification, quality metrics, risk management, quality agreements, audits and performance monitoring
Champion continuous improvement and digital transformation of Supplier Quality processes, systems and reporting
Provide technical quality leadership for nonconformance management, investigations, CAPA, change management, verification and validation, and manufacturing process controls
Partner with cross-functional teams and external manufacturers to resolve quality issues, mitigate supply and compliance risks, support product lifecycle activities and achieve business objectives
Recruit, coach and develop team members; establish training programs and foster quality, accountability and continuous improvement
Support internal audits, supplier assessments and regulatory inspections while meeting financial, GMP, health, safety and environmental commitments

Requirements

What you’ll need

University/Bachelor’s degree or equivalent in Engineering/Scientific or associated relevant Technical / Engineering discipline is required
Minimum of 6 years progressive experience in a regulated industry
Minimum of 2 years of experience in a managerial capacity
Previous work experience with Suppliers
Demonstrated knowledge of the business impact of compliance issues and risk management
Experience in leadership roles involving project management, problem solving and technical projects
Skills in negotiating and influencing decision makers, decision making, communication, judgement, tact and leadership
Up to 20% domestic and international travel may be required
Advanced degree in engineering/scientific discipline preferred
Relevant medical devices and/or pharmaceutical industry experience preferred
Supply Chain and/or R&D experience preferred
Six Sigma/Process Excellence tools, training and certification preferred

Benefits

Comp & perks

Retirement plan (pension)
Savings plan (401(k))
Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year; employees residing in Colorado – 48 hours; employees residing in Washington – 56 hours
Holiday pay, including Floating Holidays – 13 days per calendar year
Work, Personal and Family Time – up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
Inclusive interview process and disability accommodations