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Associate Quality Engineer

Job in Vadnais Heights, Ramsey County, Minnesota, USA
Listing for: MME group Inc.
Full Time position
Listed on 2026-10-11
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Production QC/QA
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below
KEY

ACCOUNTABILITIES

(The broad spectrum of items that the role is ultimately held accountable for at the end of the day. Results.)

The Associate Quality Engineer is an entry-level opportunity for an engineering professional looking to build a career in Quality Engineering within a manufacturing environment. This role provides hands‑on exposure to quality systems, process validation, root cause analysis, CAPA, continuous improvement, and manufacturing processes while working alongside experienced Quality, Engineering, and Production team members. Recent engineering graduates are encouraged to apply.

KEY RESPONSIBILITIES

(The finer details of what the role is assigned for the day-to-day activities on the job. Tasks to support results.)

  • Support development and sustaining quality activities for assigned programs, including part validation, qualification, and ongoing compliance.
  • Participate in the organization’s Stage-Gate approach to product realization and new product introduction.
  • Assist with validation activities, including IQ, OQ, and PQ protocols and reports, under the guidance of experienced Quality and Engineering team members.
  • Support quality planning activities, including Process Flow Diagrams, Process FMEAs, Control Plans, work instructions, and inspection instructions.
  • Assist with customer quality concerns, investigations, documentation, and corrective actions.
  • Participate in CAPAs, SCARs, RMAs, and other quality improvement activities.
  • Support the review and disposition of internally produced nonconforming material.
  • Work collaboratively with Manufacturing, Engineering, Production, and Supply Chain teams to identify and resolve quality issues.
  • Participate in internal, customer, ISO 13485, and regulatory audits, including audit preparation, documentation, and follow-up activities.
  • Analyze quality and production data to identify trends and opportunities to improve product and process performance.
  • Support continuous improvement initiatives using Lean/Six Sigma principles to help reduce defects, scrap, rework, and customer complaints.
  • Participate in structured problem-solving activities such as 8D, DMAIC, A3, and root cause analysis, with guidance from senior team members.
  • Assist Production, Engineering, and Processing teams with updating Control Plans, work instructions, inspection methods, and other quality documentation.
  • Support shop‑floor quality initiatives and help reinforce adherence to established processes, procedures, and quality standards.
  • Assist with NCR and MRB activities, including investigation, documentation, disposition, risk assessment, corrective actions, and closure.
  • Develop knowledge of quality engineering tools, regulatory requirements, manufacturing processes, and continuous improvement methodologies through hands‑on experience and mentorship.
LMA RESPONSIBILITIES

(Leadership, Management, Accountability)

None

QUALITIES FOR SUCCESS

(Seaway Core Values, Education, Training, Certifications, Years of experience, Other skills and abilities, Physical Requirements for the Role, etc.)

  • Demonstrates Seaway Plastics Core Values
  • We are customer focused
  • We execute
  • We win together
  • We are respectful
  • Bachelor’s degree in engineering or a related technical discipline preferred. Recent graduates are encouraged to apply.
  • 0–2 years of experience in quality, engineering, manufacturing, or a related technical environment preferred. Relevant internships, co‑op experience, or academic projects may be considered.
  • Exposure to or an interest in learning process validation activities, including IQ, OQ, and PQ.
  • Familiarity with quality systems or regulated manufacturing environments is a plus.
  • Exposure to ISO 13485, FDA quality requirements, cGMP, or cGDP is preferred but not required.
  • Basic understanding of root…
Position Requirements
10+ Years work experience
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