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 2+ 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 Don't meet every qualification?
We encourage you to apply. We're interested in candidates who are eager to learn, grow, and contribute to our team's success. Job Type & Location This is a Contract to Hire position based out of St Paul, MN. Pay and Benefits The pay range for this position is $35.00 - $65.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.
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 St Paul,MN.
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