Job Title

2 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. This range is provided by Akkodis. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range 120,000.00 / yr - $130,000.00 / yr Direct message the job poster from Akkodis Akkodis is currently seeking a Quality Manager for a medical device manufacturer in the Dayton, OH metropolitan area. The ideal candidate for this position is a detail-oriented and strategic quality professional with deep knowledge of FDA and ISO 13485 regulations, hands-on experience managing quality systems in a regulated environment, and strong leadership skills in guiding cross-functional teams. This organization offers a dynamic and mission-driven work environment, competitive benefits, and a strong commitment to innovation, compliance, and continuous improvement in the development of life-enhancing medical technologies. Salary Range : $120,000-$130,000 Key Responsibilities : Lead the implementation, maintenance, and improvement of the companys Quality Management System (QMS) in accordance with FDA 21 CFR Part 820, ISO 13485, and other applicable global regulatory requirements. Direct internal efforts related to regulatory audits, inspections, and quality system certifications. Analyze operational data related to manufacturing, product design, field performance, and market trends to inform quality strategies and risk mitigation efforts. Oversee document control processes, ensuring timely review and approval of controlled documents, records, and design history files. Manage and develop a cross-functional quality team including QA engineers, inspectors, and internal auditors. Evaluate and optimize quality control procedures for in-process and final inspections of medical devices, ensuring compliance with validated processes and product specifications. Collaborate with R&D, manufacturing, and regulatory teams to support design controls, verification / validation, and design transfer activities. Drive continuous improvement initiatives using tools such as CAPA, root cause analysis, and risk management. Review quality metrics and quality-related financial data to support budget planning and operational effectiveness. Lead cross-functional meetings to define and review quality objectives, establish interdepartmental responsibilities, and ensure alignment with business goals. Work closely with external suppliers to evaluate material compliance, capacity, and adherence to medical device quality standards (e.g., supplier qualification and audits). Partner with engineering teams to resolve quality issues across the product lifecyclefrom design through post-market surveillance. Perform other duties as required to support regulatory readiness, product safety, and organizational quality culture. Qualifications Bachelors degree in a related field required; Masters degree preferred, or equivalent combination of education and experience 6+ years of relevant experience in quality management, preferably in a regulated industry Strong verbal and written communication skills, including the ability to interpret technical documents and effectively present to senior leadership and external stakeholders Proficient in interpreting and analyzing scientific journals, legal documents, financial reports, and regulatory guidelines Advanced mathematical skills, including knowledge of statistical analysis, sampling theory, and variance analysis Strong problem-solving and analytical skills, with the ability to work with both abstract concepts and technical data Comfortable working in both office and manufacturing environments; must adhere to safety protocols on the production floor Physically capable of lifting up to 50 lbs and performing tasks requiring standing, walking, and manual dexterity Ability to travel occasionally, both domestically and internationally, to support business operations Full-time availability, Monday through Friday, with flexibility to work additional hours as needed This position is open to exceptional relocation candidates. If you are interested in this onsite position in the Dayton, OH metropolitan area, then please click APPLY NOW. For other opportunities available at Akkodis go to If you have questions about the position, please contact Ryan Miller at . Equal Opportunity Employer / Veterans / Disabled Benefit offerings include medical, dental, vision, term life insurance, short-term disability insurance, additional voluntary benefits, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State or local law; and Holiday pay upon meeting eligibility criteria. Disclaimer : These benefit offerings do not apply to client-recruited jobs and jobs which are direct hire to a client To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit : / / / en-us / candidate-privacy / The Company will consider qualified applicants with arrest and conviction records. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Quality Assurance Industries Manufacturing Referrals increase your chances of interviewing at Akkodis by 2x Sign in to set job alerts for Quality Assurance Manager roles. Quality Manager mid level ( Manufacturing mid level role) Dayton Metropolitan Area $95,000.00-$110,000.00 1 week ago Assistant Manager - Ambulatory Neurology Vice President, Branch Leader - Dayton, OH Private Equity Center of Excellence, Manager Dayton, OH $93,000.00-$171,300.00 2 weeks ago Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. J-18808-Ljbffr #J-18808-Ljbffr