Medical Device Quality Management System Specialist

Vector Surgical, LLC; Menomonee Falls (WI); On-site; USD 70,000 - 110,000; Full time

Job summary

Vector Surgical, LLC is seeking an outstanding Medical Device Quality Management System Specialist in Menomonee Falls, WI. The role supports the QMS implementation, maintenance, and continuous improvement across QA, producing quality records and coordinating audits.

The specialist collaborates with Manufacturing, Engineering, and suppliers to ensure compliance with ISO 13485, FDA regulations, and company procedures, while performing quality control testing and data analysis.

Qualifications

• BS degree with hands-on QA/QMS in regulated industry.
• Experience with ISO 13485 and FDA requirements.
• Laboratory testing and QC data handling experience.
• Audit support and supplier quality familiarity.

Responsibilities

• Maintain and improve the QMS in line with regulations.
• Prepare quality metrics, trend analyses, dashboards, and reviews.
• Manage documentation, batch records, and control activities.
• Coordinate CAPA, NCRs, SCARs, and supplier quality.

Skills

QMS

ISO 13485 familiarity

FDA QSR 21 CFR 820

Laboratory QC testing

Data analysis & reporting

Document control

CAPA & nonconformances

eQMS & ERP systems

Technical writing

Attention to detail

Cross-functional collaboration

Independent work & teamwork

Education

Bachelor's degree in Engineering/Life Sciences/ Chemistry

Minimum 3 years QA/QMS in regulated industry

Lab experience with microbiology/physical testing

Auditor training or CQE desirable

Tools

eQMS software

ERP systems

Laboratory instruments

Regulatory databases

Job description

Vector Surgical is an award-winning medical device company. Small yet dynamic, we are growing quickly and looking for an outstanding individual for our Medical Device Quality Management System Specialist.

The Quality Management System (QMS) Specialist reports to the Quality Assurance System Manager and supports the implementation, maintenance, and continuous improvement of the company's Quality Management System (QMS). This role is responsible for executing day-to-day quality system activities, maintaining quality records and documentation, coordinating quality processes, supporting audits and supplier quality activities, performing quality control testing, and data analysis. The position works independently from Production and R&D while collaborating closely with Manufacturing, Engineering, and external suppliers to ensure compliance with applicable medical device regulations and company procedures.

KEY RESPONSIBILITIES

1. Quality Management System Support

• Support the Quality Manager in maintaining and improving the Quality Management System in accordance with ISO 13485, FDA regulations, and company procedures.
• Prepare quality metrics, trend analyses, dashboards, graphs, and presentations for Management Reviews and other Quality reviews.
• Maintain quality records and ensure timely completion of routine QMS activities.
• Monitor quality system performance, identify opportunities for improvement, and support implementation of quality improvement initiatives.
• Provide quality support for production activities.
• Maintain production quality tracking spreadsheets and quality databases.
• Support process validation activities.

2. Document Control

• Develop, revise, and maintain quality system documentation, including procedures, work instructions, specifications, forms, and quality records.
• Review batch-related documentation, including Device History Records (DHR), label proofing, and quality control records for completeness and compliance.
• Coordinate document revisions and document control activities.
• Support the Quality Manager in the document approval process.

3. Quality Control

• Perform laboratory quality control activities, including internal production testing, environmental monitoring, and other laboratory analyses as applicable.
• Maintain laboratory records, quality control data, and quality logs.
• Record, analyze, and communicate quality control results; advise about trends and opportunities.
• Support investigations related to quality control findings.

4. Complaint Handling and CAPA

• Coordinate the complaint handling process from receipt through closure.
• Maintain complaint files and complaint metrics.
• Track CAPAs, nonconformances, and effectiveness verification activities.
• Participate in investigations, root cause analysis, and implementation of corrective and preventive actions.
• Support supplier qualification, ongoing supplier performance monitoring and supplier audits.
• Coordinate Supplier Corrective Action Requests (SCARs) and communicate quality nonconformances to suppliers.
• Provide quality input for supplier documentation and agreements.

6. Audits and Regulatory Compliance

• Participate in planned internal audits.
• Assist the Quality Manager in planning, coordinating, and supporting external audits and regulatory inspections.
• Maintain audit records and support follow-up of audit findings.

REQUIRED COMPETENCIES

1. Skills

• Experience using Quality Management Systems in regulated industries.
• Familiarity with medical device regulations, including ISO 13485 and FDA Quality System Regulations (21 CFR Part 820/QMSR).
• Proficient in microbiological and physicochemical testing, skilled in QC instrument operation, calibration, and troubleshooting, and versed in GMP/GLP regulatory requirements.
• Understanding of sterile medical device manufacturing, labeling, validation, and regulatory requirements.
• Knowledge of complaint handling, CAPA, supplier quality, document control, and audit processes.
• Strong analytical and data management skills.
• Excellent technical writing skills for procedures, specifications, and quality documentation.
• Attention to detail is a must.
• Ability to work independently while effectively supporting cross-functional teams.
• Proficiency with Microsoft Excel, Word, PowerPoint, electronic Quality Management Systems (eQMS), and ERP systems.
• Effective communication and interpersonal skills.

2. Qualifications

• Bachelor's degree in Engineering, Life Sciences, Chemistry, Microbiology or another related scientific discipline that includes laboratory coursework and hands-on laboratory training as part of the curriculum.
• Minimum 3 years of experience in Quality Assurance or Quality Management Systems within a highly regulated industry, preferably medical devices or pharmaceuticals.
• Minimum of 3 years of laboratory experience—whether in Quality Control, R&D, or analytical development—with hands-on exposure to both microbiological and physical/chemical testing methodologies.
• Experience supporting manufacturing and engineering teams in a regulated medical device environment.
• Internal Auditor training or certification (ISO 13485 or equivalent) is preferred.
• ASQ Certified Quality Engineer (CQE) or equivalent quality certification is desirable.

This is an office-based position located in Menomonee Falls, Wisconsin; relocation is not provided.