StaffAttract
  • Login
  • Create Account
  • Products
    • Private Ad Placement
    • Reports Management
    • Publisher Monetization
    • Search Jobs
  • About Us
  • Contact Us
  • Unsubscribe

Login

Forgot Password?

Create Account

Job title, industry, keywords, etc.
City, State or Postcode

Supplier Quality Engineer

Katalyst Healthcares & Life Sciences - Saint Paul, MN

Apply Now

Job Description

Summary: We are seeking a highly skilled and detail-oriented Supplier Quality Engineer to join our team. The ideal candidate will have a strong background in medical device supplier quality, with hands-on experience in supplier qualification, PPAP documentation, and process validation. This role is critical in ensuring that suppliers meet Healthcare's quality standards and regulatory requirements. Roles & Responsibilities: Supplier Qualification & Management: Qualify suppliers in accordance with company standards. Manage and maintain the Approved Supplier List (ASL) in compliance with Healthcare's purchasing control procedures. PPAP Documentation & Execution: Manage and release all PPAP deliverables including Control Plans, MSA, PFMEA, FAI, etc., within the document control system. Support PPAP execution with suppliers and ensure robust process qualification/validation using IQ, OQ, and PQ methodologies. Inspection & Test Method Validation: Define Receiving Inspection requirements. Validate test methods in alignment with internal Healthcare procedures. Cross-Functional Collaboration: Work with cross-functional teams to develop and implement product acceptance sampling strategies. Deploy supplier quality tools such as PFMEA, MSA, control plans for both new and legacy products. Technical Support & Quality Assurance: Provide technical assistance to suppliers throughout the product/process qualification lifecycle. Ensure delivery of high-quality parts, materials, and services to prevent defects and support Healthcare's commitment to reliability. Issue Resolution: Collaborate with suppliers to address SCAPA/Client issues in Education & Experience: Bachelor's degree in Engineering or related field. Minimum 4+ years of experience in supplier quality engineering within the medical device industry . ISO 13485 Certified Talent preferred by client. Strong knowledge of PPAP, IQ/OQ/PQ, PFMEA, MSA, and control plans. Familiarity with FDA and ISO 13485 standards. Excellent communication and problem-solving skills. Ability to work independently and in cross-functional teams.

Created: 2026-04-02

➤
Footer Logo
Privacy Policy | Terms & Conditions | Contact Us | About Us
Designed, Developed and Maintained by: NextGen TechEdge Solutions Pvt. Ltd.