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Quality Engineer I — Medical Device (Onsite — Arden Hills, MN) Possible Contract Extension

Pharmavise Corporation
Posted 4 months ago, valid for 15 days
Location

Arden Hills, MN, US

Salary

Competitive

Contract type

Contract

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Sonic Summary

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  • This 12-month contract role at the Arden Hills Post Market Complaint Investigation Site focuses on analyzing product performance data related to Interventional Cardiology & Vascular Therapies devices.
  • The position requires a Bachelor's degree in Engineering or a related field with 0-1 years of relevant experience and offers a salary of $70,000 per year.
  • Key responsibilities include analyzing post-market surveillance data, leading product signal escalations, and collaborating cross-functionally to improve processes.
  • The role emphasizes communication of product performance insights to leadership and a commitment to patient safety and product quality.
  • Preferred qualifications include experience in SAP, MES, or TrackWise, along with knowledge of Quality System Regulations and ISO13485 standards.
Job Purpose
This 12-month contract role leads technical efforts at the Arden Hills Post Market Complaint Investigation Site (CIS), focusing on analyzing product performance data to investigate and escalate issues across a range of Interventional Cardiology & Vascular Therapies (ICVT) devices. It involves cross-functional collaboration to drive product and process improvements and enhance investigation outcomes. The position also offers high visibility across site and divisional leadership.

Responsibilities:
• Analyze post-market surveillance data, including customer complaints and adverse events, to ensure timely identification, investigation, and resolution of safety or quality issues in compliance with regulatory and internal standards.
• Lead product signal escalations by conducting root cause investigations, documenting findings in the quality system, and identifying opportunities for performance improvement.
• Collaborate cross-functionally to develop and implement efficient, compliant solutions that enhance Complaint Investigation Site (CIS) processes and support organizational and regulatory goals.
• Communicate product performance insights through formal presentations to leadership and design teams, support published performance reports, and respond to customer inquiries directly or via the sales organization.
• Uphold a strong commitment to patient safety and product quality by ensuring adherence to the Quality Policy and all relevant procedures and standards.

Minimum Requirements:
• Bachelor’s degree in Engineering or a related technical or scientific discipline with 0-1 years of relevant experience
• Knowledgeable in Quality System Regulations, Medical Device Regulation, and ISO13485 Quality Standards.
• Proficient in Microsoft Word, Excel, and Outlook
• Strong attention to detail
• Solid writing and communication skills
• Apply critical thinking to ensure investigations are thorough, appropriate, and aligned with procedural and quality requirements.

Preferred Requirements:
• Experience in SAP, MES, or TrackWise




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