12,881 Supplier Quality jobs in the United States

Role Summary

The Supplier Onboarding Coordinator will support the SPS onboarding initiative by facilitating the activation of over 1,200 suppliers in a high-volume, time-sensitive environment. This role will serve as a liaison between suppliers and internal EDI teams, ensuring timely onboarding, clear communication, and resolution of escalations. They will proactively reach out to suppliers as needed to ensure onboarding momentum, clarify technical requirements, and resolve issues. This role demands a high level of responsiveness, professionalism, and clarity in both written and verbal communication.

Key Responsibilities:

The Supplier Onboarding Coordinator will be accountable for delivering weekly updates that cover:

• Supplier escalations and resolution status
• Assistance provided to suppliers and internal teams
• Communication touchpoints and outreach efforts
• Supplier connection progress and onboarding milestones
• Track onboarding milestones, escalate delays, and ensure timely resolution
• Generate and deliver onboarding metrics and progress reports
• Support ad hoc reporting and coordination requests
• Present updates and insights to internal teams with confidence and clarity

Required Qualifications:

• Proficiency in Microsoft Office Suite
• Intermediate skills in Excel (pivot tables, v-lookups) and Word
• Strong technical communication and customer service orientation
• Comfortable with public speaking and team-facing presentations
• Detail-oriented with the ability to manage multiple priorities

About Us:

Precision Tube & Catheter, Inc. (PT&C) is a high-tech enterprise dedicated to manufacturing advanced materials and components for interventional and implantable medical devices. We produce high-quality medical tubes used in various applications, including anesthesiology, respiratory equipment, and biopharmaceutical laboratory equipment. Our commitment to innovation and excellence drives us to exceed industry standards and client expectations.

Position Summary:

We are a fast-growing startup specializing in the manufacturing of high-performance components for medical catheters, including extruded tubing, shrink tubing, and braided tubing. We are seeking a hands-on and highly motivated Quality Assurance, Supplier Quality Engineering, and Quality Control (QA/SQE/QC) Engineer to lead and execute quality operations and help build a strong foundation for regulatory compliance and product excellence. The QA/SQE/QC Engineer will play a critical role in establishing and maintaining product and process quality. This position will ensure that our products meet or exceed regulatory and customer expectations, support supplier quality management, and oversee in-house quality control activities.

Key Responsibilities:

Quality Assurance (QA) – Process/System-Focused

• Develop and maintain a compliant Quality Management System (QMS) in accordance with ISO 13485 and FDA 21 CFR Part 820.
• Lead internal and external audits; manage CAPA processes and follow-up activities.
• Conduct risk assessments (e.g., PFMEA) and ensure integration of quality in product development and manufacturing.
• Write, revise, and control SOPs, work instructions, forms, and quality records.
• Support equipment and process validations (IQ, OQ, PQ) for tubing manufacturing processes.
• Participate in internal audits, customer audits, and regulatory inspections.
• Manage CAPA processes: initiate, investigate, and implement corrective and preventive actions.
• Collaborate with cross-functional teams (Engineering, Production, R&D) to identify critical-to-quality (CTQ) parameters and ensure product quality.
• Maintain and organize Device History Records (DHRs), Device Master Records (DMRs), and training logs.

Supplier Quality Engineering (SQE):

• Qualify and onboard new suppliers; perform supplier audits and evaluations.
• Define incoming inspection requirements and ensure component conformance.
• Manage supplier non-conformances; initiate and follow through on SCARs.
• Collaborate with suppliers on process improvements and corrective actions.

Quality Control (QC) – Product-Focused

• Perform incoming, in-process, and final inspections of extruded, shrink, and braided tubing.
• Conduct First Article Inspections (FAIs) and maintain inspection records.
• Develop test methods and protocols for product performance and reliability.
• Monitor production quality metrics (e.g., scrap rate, yield, defect rate).
• Maintain and calibrate inspection tools and equipment.
• Use precision measurement tools (micrometers, laser micrometers, pin gauges, tensile testers, etc.).
• Monitor visual and dimensional quality to ensure conformance to specifications and customer requirements.
• Initiate and track Non-Conformance Reports (NCRs) and assist in root cause analysis.
• Maintain calibration logs and ensure metrology equipment is accurate and up-to-date.

Qualifications:

• Bachelor’s degree in Materials Engineering, Quality, or a related technical field.
• 2+ years of experience in a QA/SQE/QC role in the medical device industry preferred.
• Familiarity with catheter manufacturing processes, especially extrusion, shrink tubing, or braiding, is a strong plus.
• Solid understanding of ISO 13485 and FDA QSR (21 CFR Part 820) requirements.
• Experience with quality tools: CAPA, FMEA, 5 Whys, Fishbone Diagram, etc.
• Strong attention to detail, documentation, and organizational skills.
• Hands-on experience with inspection techniques and equipment.
• Ability to thrive in a fast-paced, startup environment.
• Excellent communication, problem-solving, and analytical skills.

Preferred Qualifications:

• Experience with catheter manufacturing processes.
• ASQ certification (CQE, CQA, or equivalent) is a plus.
• Mandarin speaking is a plus

Working Conditions:

Work is performed in a manufacturing environment, requiring adherence to safety protocols.

May involve standing for extended periods and lifting materials as needed.

Benefits / Other:

We believe our employees are our greatest resource. We offer a competitive salary and benefits package including 401(k) with employer contribution, paid holidays, and vacation. Insurance coverage includes medical, dental, vision, and prescription drugs.We are proud to be an equal-opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If you have a disability or special need that requires accommodation, please let us know. If applying for positions in the U.S., you must be eligible to work in the U.S. without needing an employer-sponsored visa (work permit).

Why Join PT&C?

• Be part of a high-impact startup developing critical medical components.
• Work closely with founders and engineers to shape company processes and culture.
• Opportunity for rapid professional growth and ownership in building quality systems from the ground up.

To Apply:

Please submit your resume and cover letter to We look forward to reviewing your application!

Precision Tube & Catheter, Inc. ( ) is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

About Us:

Precision Tube & Catheter, Inc. (PT&C) is a high-tech enterprise dedicated to manufacturing advanced materials and components for interventional and implantable medical devices. We produce high-quality medical tubes used in various applications, including anesthesiology, respiratory equipment, and biopharmaceutical laboratory equipment. Our commitment to innovation and excellence drives us to exceed industry standards and client expectations.

Position Summary:

We are a fast-growing startup specializing in the manufacturing of high-performance components for medical catheters, including extruded tubing, shrink tubing, and braided tubing. We are seeking a hands-on and highly motivated Quality Assurance, Supplier Quality Engineering, and Quality Control (QA/SQE/QC) Engineer to lead and execute quality operations and help build a strong foundation for regulatory compliance and product excellence. The QA/SQE/QC Engineer will play a critical role in establishing and maintaining product and process quality. This position will ensure that our products meet or exceed regulatory and customer expectations, support supplier quality management, and oversee in-house quality control activities.

Key Responsibilities:

Quality Assurance (QA) – Process/System-Focused

• Develop and maintain a compliant Quality Management System (QMS) in accordance with ISO 13485 and FDA 21 CFR Part 820.
• Lead internal and external audits; manage CAPA processes and follow-up activities.
• Conduct risk assessments (e.g., PFMEA) and ensure integration of quality in product development and manufacturing.
• Write, revise, and control SOPs, work instructions, forms, and quality records.
• Support equipment and process validations (IQ, OQ, PQ) for tubing manufacturing processes.
• Participate in internal audits, customer audits, and regulatory inspections.
• Manage CAPA processes: initiate, investigate, and implement corrective and preventive actions.
• Collaborate with cross-functional teams (Engineering, Production, R&D) to identify critical-to-quality (CTQ) parameters and ensure product quality.
• Maintain and organize Device History Records (DHRs), Device Master Records (DMRs), and training logs.

Supplier Quality Engineering (SQE):

• Qualify and onboard new suppliers; perform supplier audits and evaluations.
• Define incoming inspection requirements and ensure component conformance.
• Manage supplier non-conformances; initiate and follow through on SCARs.
• Collaborate with suppliers on process improvements and corrective actions.

Quality Control (QC) – Product-Focused

• Perform incoming, in-process, and final inspections of extruded, shrink, and braided tubing.
• Conduct First Article Inspections (FAIs) and maintain inspection records.
• Develop test methods and protocols for product performance and reliability.
• Monitor production quality metrics (e.g., scrap rate, yield, defect rate).
• Maintain and calibrate inspection tools and equipment.
• Use precision measurement tools (micrometers, laser micrometers, pin gauges, tensile testers, etc.).
• Monitor visual and dimensional quality to ensure conformance to specifications and customer requirements.
• Initiate and track Non-Conformance Reports (NCRs) and assist in root cause analysis.
• Maintain calibration logs and ensure metrology equipment is accurate and up-to-date.

Qualifications:

• Bachelor’s degree in Materials Engineering, Quality, or a related technical field.
• 2+ years of experience in a QA/SQE/QC role in the medical device industry preferred.
• Familiarity with catheter manufacturing processes, especially extrusion, shrink tubing, or braiding, is a strong plus.
• Solid understanding of ISO 13485 and FDA QSR (21 CFR Part 820) requirements.
• Experience with quality tools: CAPA, FMEA, 5 Whys, Fishbone Diagram, etc.
• Strong attention to detail, documentation, and organizational skills.
• Hands-on experience with inspection techniques and equipment.
• Ability to thrive in a fast-paced, startup environment.
• Excellent communication, problem-solving, and analytical skills.

Preferred Qualifications:

• Experience with catheter manufacturing processes.
• ASQ certification (CQE, CQA, or equivalent) is a plus.
• Mandarin speaking is a plus

Working Conditions:

Work is performed in a manufacturing environment, requiring adherence to safety protocols.

May involve standing for extended periods and lifting materials as needed.

Benefits / Other:

We believe our employees are our greatest resource. We offer a competitive salary and benefits package including 401(k) with employer contribution, paid holidays, and vacation. Insurance coverage includes medical, dental, vision, and prescription drugs.We are proud to be an equal-opportunity workplace. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If you have a disability or special need that requires accommodation, please let us know. If applying for positions in the U.S., you must be eligible to work in the U.S. without needing an employer-sponsored visa (work permit).

Why Join PT&C?

• Be part of a high-impact startup developing critical medical components.
• Work closely with founders and engineers to shape company processes and culture.
• Opportunity for rapid professional growth and ownership in building quality systems from the ground up.

To Apply:

Please submit your resume and cover letter to We look forward to reviewing your application!

Precision Tube & Catheter, Inc. ( is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Akkodis is seeking a Senior Manager, Supplier Quality for a full-time job with a client in Lakewood, CO . We are seeking an experienced leader to drive supplier quality excellence across a global portfolio of contract manufacturers. This role will lead a skilled engineering team working with external manufacturing partners to ensure high-quality, compliant, and scalable delivery of complex electro-mechanical systems.

Salary Range: $160.400/year to $200,600/year. The salary may be negotiable based on experience, education, geographic location, and other factors.

Senior Manager, Supplier Quality job responsibilities include:

· Partner directly with 3rd party manufacturers responsible for manual assembly and shipment of products to customers

· Drive improvements in supplier quality while ensuring production remains high and on schedule

· Lead analysis to determine whether new products should be manufactured in-house or through external partners

· Play a pivotal role as the organization shifts from 70% sustaining products to 70% new product development

· Build KPIs, identify global trends, and conduct onsite audits to qualify and strengthen supplier capabilities

Desired Qualifications:

• Bachelor’s degree or equivalent of education and experience sufficient to successfully perform the essential functions of the job may be considered.

Bachelor of Science degree or may have a Master of Science degree, in Engineering, preferred.

· Strong collaboration and relationship management skills, with the ability to mend and strengthen supplier partnerships

· 10+ years of experience, including 5+ years in leadership roles

· Proven ability to manage contract manufacturers, evaluate supplier capacity, and balance quality with production needs

· Expertise in supplier quality engineering, process improvement, and regulatory compliance

If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at

Equal Opportunity Employer/Veterans/Disabled

Benefits offerings include but are not limited to :

• Medical
• Dental
• Vision

To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit .

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

· The California Fair Chance Act

· Los Angeles City Fair Chance Ordinance

· Los Angeles County Fair Chance Ordinance for Employers

· San Francisco Fair Chance Ordinance

Supplier Quality Manager - Extrusion*

As the Manager, Supplier Quality Commodity Manager for Extrusion, you will lead the quality initiatives for our extrusion commodity, ensuring the reliability and compliance of externally sourced components and materials. This pivotal role bridges procurement, engineering, and quality assurance, driving supplier development, risk mitigation, and continuous improvement. As the quality lead for extrusion, you’ll manage supplier performance, conduct audits, and ensure adherence to regulatory standards while supporting new product introductions and strategic sourcing decisions. If you're passionate about quality, collaboration, and innovation in a global medical device environment, we invite you to make a lasting impact with us.

ESSENTIAL DUTIES

• Develop and implement supplier quality strategies for assigned commodities working closely with supply chain and the quality assurance team.
• Drives proactive solutions and development that improve overall supplier performance. Supports supplier performance and risk processes to create predictive measures to help prevent issues that might impact our facilities or customers.
• Assume overall responsibility for the commodities quality performance within Company and in accordance with assigned KPI’s.
• Conduct supplier audits and assessments to ensure compliance with quality standards.
• Monitor, measure and action supplier performance using KPIs such as PPM, on-time delivery, and corrective action responsiveness.
• Serve as a quality expert for the specific commodity and collaborate with engineering and sourcing to define quality requirements and specifications.
• Acts as a lead for supplier quality in supplier selection. Drives the process to standard procedures, coordinates with supply chain, and holds the supplier quality team accountable to deliver quality suppliers that meet or exceed our expectations.
• Drives supplier escalations and resolution, solving problems through problem solving methodology (8D, A3, DMAIC). Monitors solutions to prevent repeat issues.
• Support supplier transfers, new product introductions, and projects that impact their commodity suppliers.
• Provides guidance and mentorship to junior members of the team on the principles of supplier management, new product design, and component qualifications.
• Instills quality processes and best practices within Client facilities and at suppliers. Assists in the development of new processes that improve supplier quality.
• Leads and manages continuous improvement activities for the supplier quality team as assigned.

MINIMUM QUALIFICATION REQUIREMENTS

Education

• Bachelor’s degree in business, supply chain, supplier quality, or operations field.
• MBA preferred.

Experience

• Minimum 7 years in similar role or related experience at a global manufacturing company.
• Experience with Extrusion.
• Preferred – Experience in Medical Device industry.

Skills

• Supplier relationship management & negotiation.
• Executive-level communication and stakeholder management in a global company.
• Excellent verbal and written communication, analytical, leadership, problem-solving and organizational skills.
• Demonstrated ability to consistently work through multiple issues by capitalizing on available resources and prioritizing accordingly.
• Demonstrated use of comprehensive analytical skills to determine alternatives and present recommendations.
• Demonstrated ability to manage multiple projects simultaneously and ability to thrive in a continuous improvement environment.
• Knowledge and use of relevant PC software applications and skills to use them effectively.

Certificates, Licenses, Registrations

Preferred, but not required: Supplier Quality Engineer, Quality Engineer, or Six Sigma.

1. Experience with Validation (IQ, OQ, PQ, TMV)
2. Thorough knowledge and experience with NPI Processes
3. Excellent organization, planning, technical writing, communication, and presentation skills
4. Experience in supplier quality and medical device industry.

Nice To Have

• Experience with Software components/suppliers.

In this exciting role as a Senior Supplier Quality Engineering, you will have responsibility for leading a Pre-Market Supplier Quality Engineering team for the CST OU. The Supplier Quality team primarily supports NPI (New Product Introduction) projects and supplier management activities and processes. The role encompasses both team leadership and individual contributor aspects to support the Supplier Quality goals and objectives.

Cranial and Spinal Technologies (CST) is redefining cranial and spinal procedures to reduce variability and improve outcomes with the goal of restoring long-term quality of life for more patients. CST is the market leader in spinal implants, robotics, and navigation. Part of the Neuroscience portfolio, CST is a Operating Unit (OU) comprised of four global businesses: Enabling Technologies, Spine & Biologics, intelligent Data Solutions (iDS), and China Cranial, Spinal, Orthopedics & Technologies.

Technologies delivers an innovative portfolio which include robotics, navigation, intra-operative imaging, advanced energy devices, cerebral spinal fluid management and critical care. The scope of this position will primarily focus on integrating Ear Nose and Throat (ENT) strategic products into Enabling Technologies Software and Platforms. Enabling.

The ideal candidate will have experience across a range of product types including: off the shelf sourced component, electro-mechanical components, software development kits (SDK), and surgical platform hardware components.

A leading medical device company is seeking a Supplier Quality Leader to oversee supplier quality operations and ensure compliance across a global supply base. This role will play a key part in supporting product development, manufacturing, and regulatory readiness.

Key Responsibilities:

• Lead supplier quality activities across multiple product lines and manufacturing sites.
• Manage supplier audits, assessments, and performance monitoring.
• Collaborate cross-functionally to support new product introductions and process validations.
• Drive resolution of supplier-related nonconformances, CAPAs, and quality issues.
• Support validation efforts including IQ/OQ/PQ, Gage R&R, and other qualification protocols.
• Ensure compliance with applicable standards (e.g., ISO 13485, FDA QSR).
• Develop and maintain quality documentation and metrics related to supplier performance.

Qualifications:

• Minimum of 10 years of experience in quality assurance or supplier quality within a regulated industry, preferably medical devices.
• Strong background in supplier management, validations, and quality systems.
• Familiarity with CAPA, NCRs, FMEAs, and root cause analysis.
• Excellent communication and leadership skills.

12-month contract, potential for extension or conversion

Onsite in Mounds View, MN

Experience: looking for level II, open to Sr level. Looking for someone with strong supplier quality background, supplier controls, component qualification, PPAP, manufacturing process knowledge and validation; project management experience. MUST have medical device experience

Can you please confirm your top 3 skills sets required?

1. Supplier Quality Experience: Supplier Controls/Component Qualification (PPAP), Process Validation knowledge
2. Project management knowledge
3. Medical Devices Experience and regulations knowledge.

Can you please confirm the 3 main responsibilities/day to day activities required for this role?

1. Establish supplier controls strategy for new or legacy suppliers from a component supplier or a contract manufacturer
2. Qualify components and execute activities from Policy -019 (Purchasing and Suppliers Controls) to support the new product development Launch
3. Root Cause Analysis Investigation for suppliers' issues or non-conformance situations identified internally.

What is your target years of experience? 4+ years of experience

Will the contingent worker be working remotely or onsite, or both? On site

Responsibilities may include the following and other duties may be assigned. Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier related problems as they occur. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation.

SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects from design to implementation while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education (typically University).

DIFFERENTIATING FACTORS

Autonomy: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / assignments.

Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments. Contributes to the completion of project milestones . May have some involvement in cross functional assignments.

Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex . Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.

Communication and Influence: Communicates primarily and frequently with internal contacts . External interactions are less complex or problem solving in nature. Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making.

Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream.

Required Knowledge and Experience: Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience. Requires a University Degree and minimum of 2 years of relevant experience

Location: Tampa Bay Area (On-site 3x/week)

Travel: Up to 50% (Continental U.S.)

Employment Type: Full-Time (Staff Augmentation or Contract-to-Hire)

About the Role

We are seeking a highly skilled and driven Supplier Quality Engineer with a strong engineering and manufacturing background to support supplier management and quality assurance in the medical device industry . This role blends tactical execution with strategic supplier development and sourcing initiatives.

Key Responsibilities

• Lead supplier quality activities to ensure parts and components meet engineering and regulatory requirements.
• Interpret and apply GD&T (Geometric Dimensioning and Tolerancing) to technical prints and specifications.
• Interface with engineering design , manufacturing , and supply chain teams to resolve quality issues and improve supplier performance.
• Conduct supplier audits and assessments in compliance with ISO 13485 and other relevant standards.
• Own supplier relationships, including performance monitoring, issue resolution, and continuous improvement.
• Identify and onboard new suppliers; support contract negotiation and supplier qualification .
• Collaborate with sourcing managers to align supplier capabilities with business needs.
• Drive root cause analysis and corrective actions for supplier-related nonconformances.

Qualifications

• Bachelor’s degree in Engineering or related technical field.
• Strong understanding of manufacturing processes , GD&T , and quality systems .
• Experience working in a medical device environment (ISO 13485 preferred).
• Proven ability to manage supplier relationships and influence cross-functional teams.
• Skilled in auditing, quality tools, and regulatory compliance.
• Excellent communication and negotiation skills.

Preferred Experience

• Prior experience in supplier quality , sourcing , or supply chain engineering .
• Familiarity with Touchpoint Medical or similar device manufacturers.
• Experience with strategic sourcing and supplier development.