Quality Control and Compliance Coordinator

Title: Quality Control and Compliance Coordinator Shift: Condensed Schedule | 9 hours per day Monday through Thursday, 4 hours on Friday Salary: $70,000 - $80,000 per year, plus a performance-based bonus; exact compensation is dependent on experience Quality Control and Compliance Coordinator Role Our client is seeking a detail-oriented professional to support their corporate compliance program and manage hands‑on quality control activities. This role exists to oversee daily quality operations—such as incoming inspection protocols, customer complaints, and quality document creation—while executing ISO 9001, ISO 13485, and FDA regulatory compliance tasks to protect product integrity. Responsibilities Collaborate closely with production, engineering, and supply chain teams to systematically investigate and resolve active quality issues Handle the customer complaint process end-to-end by conducting root-cause analyses with cross-functional teams and documenting corrective actions Provide technical support to inspectors regarding incoming material and finished product quality checks for electronic devices, cable assemblies, and medical products Create, review, and maintain vital quality documentation including procedures, inspection plans, quality records, and device history files Monitor and report on key quality metrics such as defect rates and complaint trends to actively contribute to process improvements Execute and maintain foundational elements of the Quality Management System (QMS) in accordance with ISO 9001 and ISO 13485 standards Support ongoing FDA compliance activities for medical device production to safeguard regulatory alignment Participate in internal, customer, and third-party certification audits, and assist with hands‑on preparation for formal FDA inspections Maintain regulatory filings, technical documentation, and quality records to ensure the facility remains audit-ready at all times Reporting Relationships The Quality Control and Compliance Coordinator reports directly to the Engineering Manager and works collaboratively with laboratory inspectors, engineers, and production staff. Qualifications Possess a Bachelor’s degree in Engineering, Quality Assurance, Regulatory Affairs, or a related technical field (or equivalent professional experience) Hold a minimum of 5 years of experience in quality and compliance within electronics manufacturing, preferably dealing with medical devices and cable/electronic assemblies Demonstrate a solid working knowledge of ISO 9001 and ISO 13485 requirements alongside FDA Quality System Regulations (QSR) Maintain extensive experience supporting quality inspections, managing customer complaints, and creating rigorous quality documentation Exhibit strong organizational, communication, and problem‑solving skills with a high level of attention to detail Demonstrate the ability to work collaboratively within a team environment while maintaining individual accountability for tasks Hold preferred qualifications such as ASQ certifications (CQE, CQA), regulatory affairs certifications (RAC), or familiarity with risk management (ISO 14971) Bring preferred experience with electronic components, validation processes, and statistical quality tools like SPC and Gage R&R Maintain the reliable ability to commute daily to the facility in Newbury, OH 44065 Benefits Offered This permanent position features a comprehensive benefits package including health, dental, vision, an HSA, life insurance, a 401(k) with company match, paid time off, company holidays, and clear opportunities for professional development and internal growth. Equal Opportunity Employer Our client provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. #J-18808-Ljbffr Gilder Search Group