×
Register Here to Apply for Jobs or Post Jobs. X

Supplier Quality Engineer

Job in Mounds View, Ramsey County, Minnesota, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2025-11-22
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Join to apply for the Supplier Quality Engineer role at Katalyst CRO
.

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
  • Qualify suppliers in accordance with company standards.
  • Manage and maintain the Approved Supplier List (ASL) in compliance with Healthcare’s purchasing control procedures.
  • 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.
  • Define Receiving Inspection requirements.
  • Validate test methods in alignment with internal Healthcare procedures.
  • Work with cross‑functional teams to develop and implement product acceptance sampling strategies.
  • Deploy supplier quality tools such as PFMEA, MSA, and control plans for both new and legacy products.
  • 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.
  • Collaborate with suppliers to address SCAPA/Client issues in compliance with company standards.
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.
Seniority level
  • Associate
Employment type
  • Contract
Job function
  • Quality Assurance
Industries
  • Pharmaceutical Manufacturing
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary