Supplier Quality Engineer

Job Description

Job Description

Supplier Quality Engineer

Join a team that's transforming lives through innovative medical technology. As a Supplier Quality Engineer, you'll play a critical role in ensuring the quality and reliability of components used in advanced therapies that support patients. In this highly visible role, you'll partner with suppliers, engineering teams, and cross-functional stakeholders to drive supplier excellence, support new product development, and ensure compliance with quality and regulatory standards. If you enjoy solving complex problems, influencing supplier performance, and making a direct impact on patient outcomes, we'd love to hear from you.

What You'll Do

• Lead supplier qualification, selection, and performance management activities
• Partner with suppliers to drive quality improvements and resolve manufacturing or component issues
• Support New Product Development (NPD) projects by ensuring suppliers and components meet quality and regulatory requirements
• Conduct supplier audits and assessments to ensure compliance with GMP and quality system standards
• Collaborate with Engineering teams to develop component qualification plans, acceptance criteria, and inspection strategies
• Review specifications, validation data, and quality documentation to support component approvals
• Drive root cause investigations and corrective actions related to supplier quality issues
• Develop and maintain strong supplier relationships while influencing continuous improvement initiatives
• Support Approved Supplier List (ASL) management and supplier quality programs
• Mentor junior engineers and contribute technical leadership across projects and teams

What We're Looking For Required Qualifications

• Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical field
• 4+ years of experience in Supplier Quality, Quality Engineering, Manufacturing Engineering, or a related function
• Experience working directly with suppliers on qualification, auditing, performance monitoring, and issue resolution
• Strong problem-solving and root cause analysis skills
• Excellent communication and stakeholder management skills
• Experience working in a regulated industry such as medical device, pharmaceutical, aerospace, automotive, or similar manufacturing environments

Preferred Qualifications

• Medical device industry experience
• Knowledge of GMP, FDA, ISO 13485, or related quality system requirements
• Experience with APQP, PPAP, FMEA, Control Plans, and supplier development activities
• Experience supporting New Product Development (NPD) programs
• Auditing experience, including supplier quality audits
• Knowledge of validation, component qualification, and receiving inspection processes

Why Join Us?

• Work on products that directly improve patients' lives
• Partner with global suppliers and cross-functional technical teams
• Influence quality strategy from supplier selection through product launch
• Lead meaningful quality and continuous improvement initiatives
• Grow your career within an innovative and mission-driven organization

Job Type & Location

This is a Contract to Hire position based out of Minneapolis, MN.

Pay and Benefits

The pay range for this position is $35.00 - $65.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Minneapolis,MN.

Application Deadline

This position is anticipated to close on Aug 21, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on us.fitly.work for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.