Quality Engineer

Electromed, Inc.; New Prague (MN); Hybrid; USD 70,000 - 118,000; Full time

Benefits offered by this job

Discretionary Time Off

Employee bonus plan

Flexible hybrid/remote work options

Parental leave benefits

Training opportunities

Job summary

Electromed, Inc. in New Prague, MN seeks a Quality Engineer to support supplier quality, incoming quality, and complaint activities.

You will analyze data, drive root-cause investigations, manage MRB dispositions, and partner across Operations, Regulatory, and Design Assurance to improve product quality and compliance. The role requires a Bachelor's degree and 2+ years in quality, with strong communication and problem-solving skills.

Qualifications

• Bachelor’s degree from an accredited college or university.
• 2+ years of hands-on Quality experience in supplier quality, incoming quality, complaints, nonconformance, or related activities.
• Experience with ISO9001-based standards (ISO9001, ISO13485, AS9100, or IATF16949).
• ASQ certification such as CQE/CSQP/CQA or similar preferred.
• Knowledge of ISO14971, ISO13485:2016, and FDA 21 CFR 820 preferred.
• Familiarity with Six Sigma problem solving tools.
• Good communication and multitasking abilities.

Responsibilities

• Collaborate with suppliers to resolve root causes of nonconforming material.
• Administer MRB process for disposition of rejected material.
• Maintain supplier quality performance metrics and scorecards.
• Lead audits and supplier re-evaluations.
• Support supplier corrective actions and investigations.
• Analyze incoming quality data for trends and risks.
• Support complaint handling and quality issue investigations.
• Participate in CAPA, deviation, and quality improvement activities.
• Interact with regulatory bodies during audits as needed.

Skills

Supplier quality

Quality metrics

Root cause analysis

CAPA

Quality auditing

Statistical methods

Cross-functional collaboration

Excellent communication

Education

Bachelor's degree

Tools

ISO9001

ISO13485

FDA knowledge

Job description

Beyond Competitive

People Purpose: Beyond Competitive

It is no longer ok to just be competitive regarding how we treat our people in everything we do. Our leadership team believes wholeheartedly we need to be beyond competitive and cultivate a culture of proud, driven employees who are passionate about the work they do and where they do it. Our leadership strives to unleash unsurpassed potential in every team and individual employed and owns making that happen. Sincere, Simple, Smart.

What makes us Beyond Competitive

• Discretionary Time Off
• Employee bonus plan
• Flexible hybrid/remote work options
• Full pay maternity, paternity, parental, short-term disability leaves
• Employee driven recognition program
• Access to hundreds of training opportunities
• Company paid educational assistance
• Well-being on demand
• Perks at Work
• Competitive health and welfare plans -HSA company contribution
• 401(k) company match
• Great culture and people!

The Opportunity

The Quality Engineer supports Electromed’s supplier quality execution, nonconforming material management, complaint processing, complaint investigation support, and product quality trending activities. This role partners closely with suppliers, Operations, Regulatory, Design Assurance, and Document Control to identify, investigate, and resolve quality issues affecting incoming materials, released product, and field performance. This position is based in New Prague, MN.

Job Outcomes You Must Get

Supplier Quality / Incoming Quality

• Collaborate with suppliers to resolve root cause(s) of nonconforming material.
• Administer the MRB (Material Review Board) process for determining disposition of rejected nonconforming material.
• Maintain supplier quality performance metrics and scorecards.
• Lead or participate in periodic re-evaluation and audit of suppliers.
• Support supplier corrective action activities and follow-up, as assigned.
• Analyze incoming quality data and nonconforming material trends to identify recurring issues, risks, and opportunities for improvement.
• Support supplier-related investigations and provide technical input when supplier issues may affect field performance or complaint trends.

Product Quality / Complaint Support

• Process customer complaints in accordance with established complaint handling procedures.
• Review, investigate, analyze, summarize, and report on complaint-related quality issues in partnership with the complaint handling program owner.
• Evaluate complaint information for potential linkage to supplier quality issues, incoming material issues, or manufacturing-related product quality concerns.
• Conduct complaint and product quality trend analysis and elevate significant findings to appropriate stakeholders.
• Participate in root cause investigations, risk evaluations, and corrective action activities arising from complaints and product quality issues.
• Collaborate with post-market members on complaint-related assessments, reportability support, and follow-up activities, as needed.
• Support complaint handling and related records during internal and external audits.

Product Quality / Quality Systems Support

• Analyze data obtained from nonconforming material activity, complaints, inspection results, or other quality inputs to identify unfavorable trends.
• Collaborate with cross-functional teams to support updates to risk management files, as needed.
• Participate in CAPA, deviation, nonconformance, and quality improvement activities.
• Create or edit QMS work instructions and related controlled quality documentation, as assigned.
• Directly participate in notified body, FDA, and internal audits, as needed.
• Initiate Engineering Change Orders as needed to support quality assurance initiatives.
• Interact with UL to update reports as assigned.

Job Outcomes Requirements

• Bachelor’s degree from an accredited college or university
• 2+ years of verifiable experience in a hands‑on Quality role supporting supplier quality, incoming quality, complaints, nonconformance, or related activities; medical device manufacturing experience preferred
• Experience working within a Quality Management System certified to any of the “ISO9001-based” standards (ISO9001, ISO13485, AS9100, or IATF16949)
• Preferred: ASQ certification including CQE, CRE, CSQP, CQA, CQI, CSSGB, CSSBB, or similar
• Preferred: Working knowledge of ISO14971, ISO13485:2016, and FDA 21 CFR 820
• Knowledge of formal problem-solving methods (for example, six-sigma problem solving tools and methodology)
• General knowledge of basic statistics utilized by Quality Assurance in manufacturing organizations, including (but not limited to):
• Measures of process capability (for example, Cpk or Ppk)
• Control Charts for variable data (for example, X-bar & R chart)
• Conventional measures of dispersion in a normally distributed data set
• Selecting and applying basic inspection sampling plans
• Tests for comparison of data sets (for example, T-test or ANOVA)
• Exceptional communication skills
• Ability to manage multiple priorities and drive timely follow-up on assigned quality issues
• Ability to travel The compensation range for this position is $70,000 to $118,000 annually with the final agreed upon rate to be based on individual experience, skills, and qualifications. Additional benefits include performance-based incentives, comprehensive health benefits, retirement savings options, paid time off, and opportunities for professional growth and development. Benefits eligibility and offerings may vary based on role and location.