Manufacturing Quality Specialist - Location: Mundelein, IL (Onsite) - Compensation: $25–$30/hour - Benefits: Our consultants are eligible to enroll in medical, dental and vision benefits. - Schedule: Monday–Friday, 8:00 AM–5:00 PM - Employment Type: Contract Project | Potential Contract-to-Hire - Project Duration: December 2026 – May 2027 About the Opportunity LaSalle Intelligent Solutions is partnering with a leading medical device and healthcare products organization to identify a Quality Assurance Analyst for its growing team. This individual will support quality initiatives within a regulated manufacturing environment, helping ensure products and processes meet established quality standards and regulatory requirements. This is an excellent opportunity for someone who enjoys analyzing processes, solving problems, and contributing to continuous improvement initiatives. Responsibilities - Establish and maintain quality standards for in-process manufacturing activities. - Evaluate production processes and identify opportunities for quality and operational improvements. - Support nonconformance investigations, root-cause analysis, and corrective and preventive actions (CAPA). - Assist with risk management activities and continuous improvement initiatives. - Develop and maintain quality documentation, including product specifications, Device Master Records (DMRs), design control files, and technical documentation. - Support vendor qualification, evaluation, and ongoing vendor management activities. - Develop and support testing, sampling, and training methods. - Analyze quality data, prepare reports, and communicate findings to relevant stakeholders. - Manage multiple projects and priorities while meeting established deadlines. Qualifications - At least 2 years of experience in Quality Assurance, Quality Engineering, or a related engineering function. - Experience supporting quality initiatives within a regulated manufacturing environment, ideally medical devices. - Working knowledge of FDA 21 CFR Part 820, ISO 13485, and applicable medical device quality standards. - Hands-on experience with nonconformance investigations, CAPA, root-cause analysis, risk management, and process improvement. - Intermediate to advanced Microsoft Excel proficiency, including formulas, pivot tables, conditional formatting, data analysis, and reporting. - Proficiency with Microsoft Office Suite, including Word, PowerPoint, and Outlook. - Strong analytical, organizational, and problem-solving skills. - Ability to work independently, exercise sound judgment, and manage competing priorities with minimal supervision. Additional Details - Fully onsite in Mundelein, IL. - Monday–Friday, 8:00 AM–5:00 PM. - Potential opportunity to transition into a permanent position. Interested? Apply today to learn more about this opportunity! Thank you, Giovanna Breslin
