Quality System Audits Jobs

The Distillery Quality Control Specialist role at IJW Whiskey Company involves ensuring product integrity and regulatory compliance across a rapidly expanding spirits operation. Key responsibilities include conducting daily HPLC and chemical analyses of raw materials and whiskey samples, maintaining statistical process control charts to drive yield improvements, and performing equipment calibration to meet TTB standards. The position offers the appeal of working with a dynamic team that combines over a century of industry expertise with ambitious global growth plans. The role is based on-site at the Danville campus and requires physical stamina in an industrial environment, providing an opportunity for professionals to contribute to the quality foundation of a leading independent spirits company.

The Quality Engineer role within the Quality Department focuses on managing overall product quality and process execution across the organization. Key responsibilities include developing and auditing the Quality Management System in compliance with ISO standards, leading root cause investigations for manufacturing issues, and driving continual improvement projects using Six Sigma methodologies. The position also involves supporting supplier quality, reviewing contracts, and performing hands-on testing. This opportunity appeals to candidates seeking a collaborative environment where they can utilize their engineering background to enhance customer satisfaction and reduce scrap. The work arrangement combines office-based planning with frequent visits to the manufacturing production floor.

The Quality Design Assurance Engineer I or II role serves as a core project team member within Heraeus Medevio, supporting the design and development of complex medical devices such as catheters and guidewires. Key responsibilities include collaborating across functional areas to drive project deliverables, developing quality and risk management plans, reviewing nonconforming products, and ensuring compliance with FDA and ISO regulations. The position offers an opportunity to work in a culture that values curiosity, continuous learning, and growth within a global organization dedicated to improving lives. This is an onsite position based in Fridley, Minnesota, with occasional travel required to the White Bear Lake location.

The Quality Engineer role at Norman Noble involves supporting a team dedicated to manufacturing life-sustaining medical devices. Key responsibilities include leading process improvement projects, managing quality system documentation and records, and collaborating with customers and suppliers on validation activities and audits. The position requires analyzing data to drive decisions and ensuring compliance with industry standards like ISO 13485. This opportunity is appealing due to the company's entrepreneurial culture where individual contributions are highly visible, the access to state-of-the-art facilities, and the focus on continuous growth through high-tech problem-solving. The role is based on-site within the company's manufacturing facilities.

The Quality Manager role leads the Quality department within a precision machining environment, reporting directly to the General Manager. Key responsibilities include developing and maintaining IATF 16949 and ISO 9001 compliance systems, leading the quality team through mentorship and training, and driving continuous improvement initiatives using Six Sigma and Lean methodologies. The position involves overseeing control plans, managing root cause analysis for defects, and serving as the primary liaison for customer and supplier quality audits. This opportunity appeals to professionals seeking a leadership position in a dynamic manufacturing setting where data-driven decision-making and cross-functional collaboration are central to operational success.

The Quality Engineer role at U.S. Tsubaki Automotive supports an international tier-one supplier by ensuring internal and customer quality standards within the automotive manufacturing sector. Key responsibilities include leading continuous improvement initiatives, conducting IATF 16949 and layered process audits, and implementing digital solutions to replace paper-based record keeping. The position requires coordinating with production and engineering teams to resolve root causes and drive corrective actions. This opportunity appeals to professionals seeking a collaborative environment focused on excellence and innovation, offering significant growth potential through leadership in quality systems. The role is based on-site at the manufacturing facility.

The Engineer, Supplier Quality role at Globus Medical focuses on managing supplier quality systems to ensure the safety and reliability of medical devices for patients with musculoskeletal disorders. Key responsibilities include evaluating and qualifying suppliers, conducting audits, and leading corrective actions for non-conformances using structured problem-solving methodologies. The position requires collaboration with Quality Engineering, Supply Chain, and Product Development teams to drive continuous improvement and compliance with international regulations. This opportunity appeals to candidates seeking to contribute to a mission-driven culture that values innovation, teamwork, and urgent patient care. The role involves domestic and international travel and offers a dynamic environment where technical expertise directly impacts surgical outcomes.

The Design Quality Engineer role supports Enovis's medical technology division by ensuring product safety, quality, and regulatory compliance throughout the design and manufacturing lifecycle. Key responsibilities include leading risk analysis through DFMEAs, authoring quality procedures and work instructions, and serving as a subject matter expert during ISO and FDA audits. The position also involves reviewing design documentation, managing nonconforming materials, and driving corrective actions for device failures. This opportunity appeals to candidates seeking to contribute to a mission-driven culture focused on improving patient outcomes through continuous innovation. The role offers a collaborative environment within a global organization, requiring minimal travel and providing a clean, professional office setting.

The Associate Director, Global Quality Operations role leads initiatives to drive operational excellence and optimize quality system processes within a global pharmaceutical organization. Key responsibilities include developing proactive risk management frameworks aligned with ICH Q9 principles, overseeing the design and standardization of global quality systems such as deviation management and CAPA, and ensuring compliance with international regulatory requirements like FDA and EMA standards. The position offers the appeal of leading digital transformation efforts in a collaborative, matrixed environment while fostering a culture of continuous improvement and patient-centricity. This strategic leadership role supports cross-functional alignment across Supply Chain and Regulatory Affairs to enhance efficiency and accountability worldwide.

The Associate Director, Global Quality Operations leads initiatives to drive operational excellence and optimize quality system processes within a global pharmaceutical organization. Key responsibilities include developing proactive risk management frameworks aligned with ICH Q9 principles, overseeing the design and standardization of global quality systems such as deviation management and CAPA, and ensuring compliance with international regulatory requirements like FDA and EMA standards. The role involves leading cross-functional collaboration to streamline workflows and supporting digital transformation efforts. This position offers the opportunity to work in a matrixed global environment where strategic thinking and process improvement methodologies directly impact patient safety and business goals. The role emphasizes a culture of respectful collaboration, empowered professional development, and impactful communication across diverse teams.

The Software Compliance Engineer role supports the Software Quality Assurance team within Abbott's Diabetes Care division in Alameda, California. This position ensures that medical device software and firmware meet strict regulatory standards, including FDA QSR and ISO guidelines. Key responsibilities include reviewing change plans and test reports to verify compliance, managing defect tracking processes, and serving as a subject matter expert during internal and external audits. The role involves active participation in Agile development cycles and collaboration with cross-functional engineering teams. This opportunity appeals to candidates seeking to contribute to life-changing healthcare technologies while working in a globally recognized company that values diversity and professional growth. The position requires occasional travel and is based at the Alameda facility.

This full-time New Product Manufacturing Engineer role within CACI's Optical and Photonic Solutions team focuses on transitioning custom photonic hardware from design to low-rate production for US Government applications. Key responsibilities include leading product transitions, developing production plans and work instructions, and overseeing laboratory technicians in building high-power photonic sources. The position requires coordinating with cross-functional teams to ensure quality compliance and schedule adherence. The role offers a flexible work arrangement with up to 10% local travel and appeals to candidates seeking a culture of integrity and continuous growth. Employees benefit from autonomy, robust learning resources, and a mission-driven environment dedicated to national safety.

This full-time Warehouse Clerk role operates on the second shift at Kenco Logistics, a leading third-party logistics provider. The position focuses on inventory control and shipping operations, with key responsibilities including reading customer orders, preparing materials for shipment, creating shipping documentation, and performing daily cycle counts to verify physical inventory against system records. The role requires utilizing warehouse management systems and maintaining a clean, safety-compliant work environment. The position appeals to candidates seeking a supportive culture that values innovation, integrity, and employee growth within the supply chain industry. It offers a stable career path with opportunities for continuous improvement and professional development in a non-travel environment.

The Field Service Technician role involves installing, inspecting, and troubleshooting power distribution equipment for clients in construction, engineering, and renewable energy sectors. Key responsibilities include performing electrical system audits, interpreting blueprints and technical manuals, documenting service reports, and providing training to customers on equipment operation. The position requires 50% travel across multiple regional locations with a flexible schedule that may include nights and weekends. This opportunity is appealing due to the company's recognized culture of care, extensive career development programs, and a merit-based environment that rewards top performers with robust benefits and growth potential.

The Industrial Construction Superintendent II role at Kelley Construction involves leading heavy industrial civil and structural projects across the Oil & Gas, Petrochemical, Energy, and Renewals sectors. The position requires managing on-site teams of 25 to 75 personnel, overseeing earthwork, foundations, and structural steel while ensuring strict adherence to safety, quality, and schedule requirements. Key responsibilities include coordinating with project managers and clients, tracking labor productivity, managing subcontractors, and maintaining detailed project documentation. This full-time opportunity offers the appeal of working with a multi-faceted general contractor known for technical expertise in complex industrial builds. The role is designed for professionals seeking dynamic field leadership with significant travel requirements, potentially up to 100%, and includes comprehensive benefits such as health insurance, retirement plans, and paid time off.

The Senior Manager, MRI Safety Engineering role leads the MRI Safety Engineering team within Abbott's Neuromodulation Division in Plano, Texas. This position provides strategic technical leadership to ensure the safety and regulatory compliance of implantable medical devices in MRI environments. Key responsibilities include defining MRI safety strategies, overseeing RF exposure analysis and testing, managing a team of engineers, and collaborating with cross-functional partners to integrate safety requirements throughout the product lifecycle. The role appeals to candidates seeking to drive innovation in life-changing healthcare technologies while working within a globally recognized company known for its commitment to diversity, career development, and a collaborative culture. The position involves occasional travel and is based on-site.

This Staff Quality Assurance Engineer role within the Manufacturing department focuses on ensuring compliance and operational efficiency in a high-mix hardware environment. Key responsibilities include managing the Quality Management System, leading internal and external audits, and serving as the subject matter expert for Electrostatic Discharge prevention. The position also involves facilitating quality review meetings, conducting root cause analyses, and driving continuous improvement initiatives using Six Sigma and Lean methodologies. The role is appealing due to the opportunity to work with a collaborative team on career-defining projects that build global technology infrastructure. It offers a fast-paced culture that values innovation and learning, with a strong emphasis on professional development and cross-functional collaboration.

The Quality Assurance Technician role at Choctaw Defense Manufacturing ensures product integrity through rigorous inspection of raw materials, components, and finished goods. Key responsibilities include performing dimensional accuracy checks using precision instruments, documenting quality data, and collaborating with cross-functional teams to resolve deviations and drive continuous improvement. The position requires a Certified Welding Inspector credential and involves conducting internal audits while maintaining detailed records of testing results. This opportunity appeals to detail-oriented professionals seeking to contribute to a culture of operational excellence within a dynamic manufacturing environment. The role is based on-site at the facility, requiring physical stamina for extended periods on the production floor while utilizing advanced quality management systems.

This onsite Senior Regulatory Affairs Specialist role within Medtronic's Pelvic Health Operating Unit supports the Neuroscience organization by ensuring compliance for minimally invasive neuromodulation therapies. The position involves coordinating document packages for regulatory submissions, managing license renewals, and recommending changes to labeling and clinical protocols to meet global standards. Key responsibilities include leading interactions with regulatory agencies and maintaining tracking systems for audits and inspections. The role appeals to professionals seeking to advance patient care for complex neurological conditions within a culture that values innovation, cross-functional collaboration, and in-person teamwork. Candidates will work onsite a minimum of four days per week to foster professional growth and contribute to a mission of alleviating pain and restoring health.

The Quality Technician role supports the Quality Management System within a manufacturing environment by collaborating with Engineering and Production teams. Key responsibilities include performing incoming, in-process, and final inspections using precision tools to verify dimensional and functional requirements, maintaining accurate documentation for audits and compliance, and initiating corrective actions for nonconforming materials. This position offers an opportunity to work in a detail-oriented setting where continuous improvement and ISO 9001 standards are prioritized. The role is ideal for individuals with a strong focus on accuracy who enjoy solving quality issues and contributing to a safe, efficient shop floor culture.

The Quality Manager role oversees the company's Quality Management System within the manufacturing division, ensuring products meet customer and regulatory standards. Key responsibilities include coordinating with Sales, Purchasing, and Operations to resolve quality issues, conducting audits and capability studies, and leading root cause investigations for customer claims. The position also involves developing standard operating procedures, managing supplier selection, and serving as a training resource for lean manufacturing principles. This opportunity appeals to professionals seeking to drive operational excellence in a mission-driven organization that values integrity and long-term relationships. The role is based in the Wichita area with a standard Monday to Friday schedule and requires travel between work sites.

The Quality Manager role at Trelleborg Marine & Infrastructure involves defining and maintaining the Quality Management System to ensure compliance across manufacturing operations. Key responsibilities include leading internal and external audits, managing nonconformance and corrective action processes, and overseeing supplier quality requirements. This position offers the opportunity to work independently with full authority over product acceptance decisions within a collaborative, international industrial environment. The role is appealing due to the company's commitment to employee growth, investment in training, and a congenial working atmosphere that values integrity and analytical problem-solving.

This senior engineering role focuses on defining and executing quality processes for cable and wire harness sub-systems within a defense technology organization. The position involves collaborating with product and manufacturing teams to drive supplier development, design functional test processes, and manage supplier qualification activities such as PPAP and audits. Key responsibilities include leading root cause analysis for fitment issues, ensuring compliance with AS9100 standards, and mitigating supply chain risks to guarantee reliable component delivery. The role appeals to candidates seeking to build world-class quality systems while working hands-on with engineering teams. It offers the opportunity to drive strategic goals across the product lifecycle with a requirement for significant travel to supplier locations and the necessity of holding a TS/SCI security clearance.

The Quality Control Manager role leads the Quality department within Havis's manufacturing facilities, reporting directly to the Plant Manager. Key responsibilities include supervising and mentoring direct reports, conducting root cause analysis to resolve customer complaints, and leading quality improvement projects and internal audits. The position also involves managing documentation for regulatory compliance and collaborating with cross-functional teams to enhance product manufacturability. This opportunity appeals to candidates seeking a dynamic environment within a fast-growing company that values innovation and safety. The role offers a collaborative culture, comprehensive benefits including health coverage and a 401(k) match, and the chance to work with cutting-edge mobility solutions in a niche market.

The Packaging Quality Supervisor role is a full-time position within the Quality department at a beverage facility in Rochester, NY. This leader oversees packaging quality functions, manages a team of analysts, and ensures compliance with FDA and TTB regulations. Key responsibilities include directing product safety testing, leading root cause investigations for quality issues, maintaining laboratory operations, and facilitating new product commercialization. The position offers a collaborative culture focused on continuous improvement and community involvement, supported by flexible scheduling, generous paid time off, and comprehensive benefits. While primarily based on-site, the role includes occasional travel to suppliers and customers for technical support and audits.