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Logistics Quality Process Analyst Jobs (NOW HIRING)

Stryker Group

Staff Engineer Quality Process

Chandler, AZ · On-site

$89K - $148K/yr

May manage audit logistics and/or preparation. * Aids in the development of validation strategies ... Strong analytical skills. * Demonstrated ability to successfully manage and complete projects in a ...

Label Aid

Quality & Process Manager

Huron, OH · On-site

Ability to analyze quality and production data, identify trends, and translate findings into ... The opportunity to help shape processes, technology, training, and quality standards across the ...

Innovar

Senior Process Analyst

Atlanta, GA · On-site

Sr. Process Analyst - Consultant The Sr. Process Analyst is responsible for leading or beingpart of ... Interact with impacted business areas to ensure accuracy and quality of future state processes ...

Innovar

Senior Process Analyst

Houston, TX · On-site

Sr. Process Analyst - Consultant The Sr. Process Analyst is responsible for leading or beingpart of ... Interact with impacted business areas to ensure accuracy and quality of future state processes ...

IT-Strat

Business Process Analyst

Falls Church, VA · On-site

$65K - $87K/yr

Business Process Analyst Falls Church, VA 8 days ago Requisition ID: 1311 Information Technology ... Defense Logistics Agency (DLA) and many others. We maintain relationships with multiple large ...

IT-Strat

$45K - $60K/yr

Business Process Analyst Falls Church, VA 8 days ago Requisition ID: 1311 Information Technology ... Defense Logistics Agency (DLA) and many others. We maintain relationships with multiple large ...

Nelson Global Products Inc.

Analyze manufacturing and quality data to reduce COPQ and improve process capability * Support Layered Process Audits, Process Audits, and IATF 16949 compliance * Support implementation and ...

BLDG SVC 32 B-J

Business Process Analyst

Manhattan, NY · On-site

$90K - $100K/yr

With the Process & Quality Engineering team the Business Process Analyst will research and design new projects, prepare and present new ideas to improve current processes. This will include analyzing ...

MM International

Business Process Analyst

Las Vegas, NV · On-site

$58K - $78K/yr

The ideal candidate will analyze, design, and optimize business processes to enhance operational efficiency, productivity, and quality. This role involves working closely with cross-functional teams ...

CSAT Solutions

Sr. Quality Process Engineer

Houston, TX · On-site

Performs statistical analysis of processes, through the use of trend charts, control charts, Pareto ... Mentor engineers and others in quality methodologies * Responsible for meeting ISO 9001 and/or ...

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Logistics Quality Process Analyst information

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How much do logistics quality process analyst jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for logistics quality process analyst in the United States is $32.41, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $37.02 per hour, depending on experience, location, and employer.

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Infographic showing various Logistics Quality Process Analyst job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 86% Full Time, 6% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $67,422 per year, or $32.4 per hour.

Staff Engineer Quality Process

Chandler, AZ • On-site

Stryker Group
IT Services • 1 - 10 employees
Learn more about Stryker Groupexternal

$89K - $148K/yr

Other

Posted 11 days ago

Job description

The Staff Quality Process Engineer will provide quality engineering leadership and direction in quality assurance, control, and preventative activities with a focus on continuous improvement of products and processes. Advocate and lead the execution of initiatives and projects to enhance quality performance within the business and for our customers. Mentor and provide technical direction across multiple areas of expertise. Ensure compliance with regulations and standards. This role is Onsite in Chandler, Arizona.

What you will do
  • Work closely with operations and the business functions to ensure quality performance of product and processes.
  • Work closely with customers, sales/marketing/field personnel, and cross-functional teams to address top quality issues.
  • Mentors, provides oversight and approval of NC/CAPA, activist and high-level expert in problem-solving and root-causing activities.
  • Initiates and leads in the development and improvement of the manufacturing processes for existing products.
  • Oversight and leads investigations during concession management.
  • Review and approval of change management activities, challenges effectiveness and drives strong review.
  • Interpret KPI trends, drive continuous improvement process.
  • Advocate of Human Factor practices, proficiency in the science of identification of mitigation.
  • Subject matter expert in risk management practices and concepts.
  • Develop and provide input by identifying opportunities and weaknesses.
  • Proficiency in and provides technical direction in optimization of inspection methods and sampling.
  • High proficiency in statistical methods and application.
  • Engage in and may lead internal and external audits with regulatory representatives, providing effective narrative and description of topic of expertise and overview of the business.
  • May manage audit logistics and/or preparation.
  • Aids in the development of validation strategies for existing products.
  • Support manufacturing transfers to other plants/facilities, leading quality activities.
  • Responsible for initiation, internal containment, and support of ship and product holds for potential product escapes.
  • Coach and mentor others in quality topics and activities.
  • Some travel may be required.
What you need
  • Bachelor of Science in engineering or related discipline.
  • Minimum of 5+ years' experience.
  • Previous medical industry experience required.
  • Understanding of US and International Medical Device Regulations.
  • Pervious product transfer experience required.
  • Familiarity with ISO 13485, GDP, GMP required.
  • Strong knowledge of Quality Concepts ( e.g. Risk Management, CAPA, Audits, Statistics).
  • Must possess strong communication, project management and influencing skills as well as have the ability to manage multiple tasks simultaneously.
Preferred
  • MS, CQE, or CRE.
  • Six Sigma Green or Black belt.
  • Experience in launching new production lines desired.
  • Experience in interacting with regulatory agencies (FDA, MoH, TUV; etc.) desired.
  • Ability to represent Quality function within and across project teams.
  • Strong interpersonal skills, written, oral communication and negotiations skills.
  • Strong in critical thinking and "outside the box" thinking.
  • Highly developed problem-solving skills.
  • Strong analytical skills.
  • Demonstrated ability to successfully manage and complete projects in a matrix organization.
  • Demonstrated ability to work independently and as part of cross-functional teams.
  • Experience in working in a compliance risk situation.
United States of America Pay Ranges:
  • USN: $89,300 - $148,800 USD Annual

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