Senior Supplier Quality Engineer jobs in United States
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Johnson & Johnson · 2 hours ago

Senior Supplier Quality Engineer

Johnson & Johnson is a leader in healthcare innovation, striving to develop smarter and less invasive treatments. The Senior Supplier Quality Engineer will oversee supplier-related quality engineering activities, ensuring compliance with industry standards and supporting new product development and manufacturing processes.

Hospital & Health Care
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

Issues resolution with suppliers – investigating challenging issues with significant business impact
Developing and maintaining suppliers – executing Supplier Reviews, audit related activities and deep dive Technical Assessments at suppliers
Development/negotiation of Quality Agreements with suppliers
Changing the way we do business – continuously improving our policies and procedures
Supplier process changes – assessing, documenting, validating, and leading or approving significant changes in supplier processes (including component approval activities)
Stabilizing new products at suppliers – working with NPD and suppliers to ensure a smooth product launch from a supplier perspective, through both pre- and post-launch activities
The technical liaison, as needed, between product development, manufacturing, external manufacturers & suppliers
Provide leadership in design & implementation of world-class quality engineering to support the entire product life cycle with focus on quality engineering activities such as root cause analysis, corrective/preventive action, risk management, analytics/statistical techniques, verification & validation, and design control across the lifecycle of the product
Provide leadership and technical expertise to ensure supplier conformance to applicable ISO, FDA (Food & Drug Administration) & MDD (Medical Devices Directive) requirements

Qualification

Quality EngineeringISO knowledgeFDA regulationsRoot Cause AnalysisSix Sigma certificationStatistical techniquesProcess ValidationAuditing experienceAnalytical ReasoningCustomer CentricityData SavvyDocument ManagementFinancial CompetenceLean Supply Chain ManagementProcess ImprovementsQuality Control (QC)Quality StandardsQuality Systems DocumentationQuality ValidationSTEM ApplicationSupervisionSupply PlanningTechnologically Savvy

Required

A minimum of a Bachelor's degree is required
A minimum of 2 years Quality/Manufacturing experience or related experience is required
It is required to be able to communicate effectively at all levels within Quality as well as cross functionally with departments such as R&D, Operations, Medical Affairs, Compliance, Manufacturing, etc
Strong root cause analysis skills are required

Preferred

A degree concentration in Engineering, Life Science, Physical Science and/or related is preferred
An advanced degree is preferred
Experience in the medical device, pharmaceutical or other highly regulated industry is preferred
Knowledge of ISO and/or cGMP regulations is preferred
Experience in a FDA regulated environment is preferred
An ASQ certification (CQE, CQM, CRE or CQA) is preferred
Six Sigma (Green Belt, Black Belt, etc.) or Process Excellence certification is preferred
Basic knowledge in Statistics, Sampling Planning, Risk Assessment and Process Validation is preferred
Auditing experience is preferred
Strong quality engineering skills with a proven track record in design verification/validation, process verification/validation, and effects analyses is strongly preferred
Analytical Reasoning, Coaching, Customer Centricity, Data Savvy, Document Management, Financial Competence, Good Automated Manufacturing Practice (GAMP), Lean Supply Chain Management, Process Improvements, Quality Control (QC), Quality Services, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy

Benefits

Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
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 period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year

Company

Johnson & Johnson

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At Johnson & Johnson, we believe health is everything.

H1B Sponsorship

Johnson & Johnson has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (48)
2024 (56)
2023 (58)
2022 (59)
2021 (44)
2020 (27)

Funding

Current Stage
Late Stage

Leadership Team

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Alex Gorsky
Former Chairman and CEO, Johnson & Johnson
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Joaquin Duato
Chairman of the Board and Chief Executive Officer
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Company data provided by crunchbase