Quality Manager at SCHLEIFRING MEDICAL SYSTEMS, LLC

Elgin, Illinois, United States -

Full Time

Start Date

Immediate

Expiry Date

11 May, 26

Salary

0.0

Posted On

11 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, AS9100 Compliance, ISO 9001 Compliance, Regulatory Requirements, Continuous Improvement, Internal Audits, Supplier Audits, Document Control, CAPA Management, Root Cause Analysis, Risk Management, Team Leadership, Lean Manufacturing, Six Sigma, Statistical Process Control, Supplier Qualification

Industry

Medical Equipment Manufacturing

Description

Description JOB TITLE: Quality Manager REPORTS TO: Managing Director FLSA STATUS: Exempt FULL TIME and on site in Elgin, Illinois ***Please note: SMS does not offer relocation packages or visa sponsorship for this position. Candidates must be authorized to work in the U.S. and able to commute to our Illinois location.*** SUMMARY: The QA Manager is responsible for overseeing the Quality Assurance function for a manufacturing organization producing precision components for medical devices. This role ensures compliance with AS9100, ISO 9001, and applicable regulatory requirements, while driving continuous improvement initiatives to maintain product integrity and customer satisfaction. In this role they will work closely with Materials, Engineering, Production and Quality to ensure Quality Programs’ accuracy. ESSENTIAL DUTIES AND RESPONSIBILITIES: · Maintain and continuously improve the QMS to ensure compliance with AS9100 and ISO 9001 standards. · Manage internal audits, supplier audits, and coordinate external audits (registrar, regulatory bodies). · Ensure proper document control, record retention, and configuration management · Ensure adherence to customer-specific requirements and applicable regulatory standards. · Oversee Corrective and Preventive Actions (CAPA), Non-Conformance Reports (NCR), and root cause analysis. · Monitor compliance with risk management and traceability requirements for components. · Lead, mentor, and develop QA team members, including quality engineers, inspectors, and technicians. · Provide training on quality standards, inspection techniques, and continuous improvement tools. · Oversee incoming material inspection, in-process quality checks, and final product release. · Review and approve quality plans, inspection criteria, and validation protocols. · Ensure proper calibration and maintenance of measuring equipment. · Drive initiatives using Lean, Six Sigma, and other quality tools to reduce defects and improve efficiency. · Implement metrics and dashboards to monitor quality performance and trends. · Manage customer complaints and ensure timely resolution with root cause analysis and corrective actions. · Evaluate and qualify suppliers, monitor supplier performance and compliance with quality standards. · Supervise QA staff, including inspectors and quality engineers. · Provide training on quality standards, procedures, and best practices. · Any and all duties assigned. Requirements QUALIFICATIONS: To perform this job successfully, an individual must possess the skills, training and abilities listed below: Education/Experience · Bachelor’s degree in engineering, Quality Management, or related field · 4–10 years related experience and/or training, or equivalent combination of education and experience. · Strong knowledge of lean manufacturing, Six Sigma, and continuous improvement methodologies · Strong knowledge of AS9100, ISO 9001 and FDA requirements. · Experience with audits, CAPA, risk management and validation of processes · Familiarity of ERP and QMS software systems. · Aerospace experience or knowledge helpful · Excellent problem-solving, communication, and organizational skills · Ability to manage multiple projects and work in a fast-paced environment Math Ability · Ability to perform calculations related to measurements, tolerances, and production quantities. · Understanding ratios, proportions, and percentages for yield and defect analysis. · Ability to interpret control charts, histograms, and Pareto charts. · Experience with trend analysis and root cause analysis using quantitative data. · Knowledge of statistical process control (SPC). · Understanding of units, conversions, and precision measurements. · Familiarity with geometric tolerancing and dimensional inspection. Reasoning Ability · Demonstrates the ability to analyze inventory inaccuracies and reason through possible causes of inaccurate counts. · Must be able to grasp Production’s processes and procedures as a means to determine root causes. Computer Skills · Knowledge of Inventory software; Manufacturing software; Order Processing systems; Payroll systems; Project Management software; Spreadsheet software, QMS Systems, and Statistical Software Minitab. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. · The employee is occasionally exposed to wet and/or humid conditions; working near moving mechanical parts; outdoor weather conditions which can include extreme cold and heat during peak times of the year. · Noise level in the work environment is moderate. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by the employee to successfully perform the essential functions of this job: · Person must sit; use hands to enter data; hear doorbells and equipment moving around them. Frequently required to reach with hands and arms; required to stand, walk, climb, stoop and kneel at times. · Person must regularly lift and/or move up to 25 pounds, frequently lift and/or move up to 50lbs; and often move 75+ pounds using lift equipment provided. · Specific vision abilities required by this job include close vision, distance vision, peripheral vision and depth perception. ADA Language (Americans with Disabilities Act) “Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job.” EEO Statement (Equal Employment Opportunity) Schleifring Medical Systems, LLC. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other legally protected status.” Benefits Paid time off (PTO) 10 Paid Holidays Company Bonus Plan 401 (K) Plan Medical, Dental, Vision and Life Insurance Voluntary Benefits: Accident/Critical Illness/Hospital Indemnity Benefits, Identity & Fraud Protection and Legal Plans Tuition reimbursement Flexible Spending Account (FSA) Employee Assistance Program Short-Term and Long-Term Disability

Responsibilities

The Quality Manager oversees the Quality Assurance function for a medical device component manufacturer, ensuring compliance with AS9100, ISO 9001, and regulatory standards while driving continuous improvement initiatives. This role involves managing audits, overseeing CAPA/NCR processes, leading the QA team, and ensuring quality checks across material inspection, in-process, and final product release.