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Lead and improve supplier quality for a global manufacturing company, ensuring top-tier performance across products and processes. Collaborate cross-functionally and drive continuous improvement while supporting innovative new product launches.
This role manages and develops all aspects of the Quality Management System, including in-process inspections, CMM operation, first article inspections, and non-conformance resolution. It combines hands-on work on CNC-machined components with process improvement, data analysis, and collaboration with production to maintain high-quality standards.
The Senior Quality Engineer ensures the highest quality standards for advanced micromanufactured components used in medical devices, focusing on compliance, process improvement, and defect prevention. The role involves collaborating with cross-functional teams to develop and validate robust quality systems, driving innovation in medical device manufacturing.
The Quality Engineer involves managing quality operations for specific value streams by developing and maintaining quality standards, systems, and procedures. Key responsibilities include conducting statistical analyses, driving continuous improvement initiatives, ensuring compliance with industry standards (e.g., ISO9001, AS9100), and collaborating with customers, suppliers, and internal teams to enhance product and process quality.
Lead and enhance quality systems for a rapidly growing manufacturing operation with a strong presence in industrial, transportation, medical, and consumer markets. Drive improvements, oversee compliance, and shape the future of quality management during a period of expansion.
The Quality Manager role at my client involves ensuring compliance with quality management systems, driving continuous improvement initiatives, and conducting thorough root cause analyses. Candidates are expected to leverage their engineering background and experience in the power electronics industry to enhance product quality and support my client's commitment to innovation and excellence.
Our client is looking to bring on a certified lead auditor for ISO9001 to work towards certification as well as managing all qualtiy control and assurance activity
Our client is located in the Wood Dale, IL location and is an established machined metals manufacturer that has been in business over 50 years. They are currently looking for another Quality Manager to join their growing business as they venture more into the aerospace industry.
Are you a Quality Supervisor who has 5+ years of experience within the Aerospace Manufacturing industry? Do you have 5+ years of managerial experience? Do you have ISO 9001 experience? If so, please read on and apply to the Quality Supervisor - Aerospace Manufacturing job based near Essex, CT.
My client is a packaging manufacturer for the pharmaceutical industry and is looking for a Senior Quality Manager due to steady growth they've been experiencing as an organization. The Senior Quality Manager will be primarily responsible for ensuring compliance with regulations and documentation and overseeing all quality activities at the facility.
This role leads the Quality department to ensure top-tier product quality, reliability, and compliance. You'll manage a team, drive continuous improvement, and oversee quality processes across multiple manufacturing programs.
Drive and improve quality processes in a precision manufacturing setting, ensuring top-tier product standards. Collaborate with internal teams and suppliers while gaining exposure to automotive and advanced manufacturing projects.
Join a precision manufacturing leader as a Quality Engineer, ensuring compliance with strict customer and industry requirements. This role blends hands-on inspection work with opportunities to improve processes, reduce defects, and maintain world-class quality standards.
My client is looking for a Quality Engineer to join their growing site in Torrington. This professional will be responsible for a variety of tasks including tooling and component inspection, quality improvement, and gauging instruments. The main focus will be to assure that all products meet all customer requirements.
Are you a Quality Engineer who has 3+ years of experience within the Medical Device Manufacturing Industry or another highly regulated industry? Do you have ISO 13485 experience and experience with lean manufacturing? Do you have a degree in engineering or a related field? If so, please read on and apply to the Quality Engineer - Medical Device Manufacturing job based near Torrington, CT.
Are you a Quality Engineer with 5+ years of experience ideally within the Power Systems Manufacturing industry? Do you have a degree in Engineering or a related field? Do you have the ability to read mechanical and schematic drawings, engineering specifications and interpret assembly and component drawings? If so, please read on and apply to the Senior Quality Engineer - Power Systems Manufacturing opening based near Danbury, CT.
Are you a Quality Engineer who has 3+ years of experience ideally within the Electronics Manufacturing industry? Do you have ISO9001 and/ or AS9100 experience? Do you have IPC or JSTD experience? Do you have a degree in Engineering or a related field? If so, please read on and apply to the Quality Engineer - Electronics Manufacturing job based near Danbury, CT.
Are you a Quality Manager with 5-10+ years of experience leading a Quality department within the Precision Manufacturing industry? Do you have ISO 9001 and/or IATF 16949 experience? Do you have managerial experience and a degree in engineering? If so, please read on and apply to the Quality Manager - Precision Manufacturing job opening based near New Haven, CT.
Are you a Quality Engineer who has 3+ years of experience within the Automotive Manufacturing industry? Do you have experience with PPAP's? Do you have a degree in engineering or a related field? Do you have experience with ISO 9001 and IATF 16949? If so, please read on and apply to the Quality Engineer - Automotive Manufacturing job based near New Haven, CT.
The Supplier Quality Engineer (SQE) oversees the quality performance of global suppliers, leading audits, corrective actions, and improvement initiatives to ensure materials and components meet specifications and regulatory requirements. This role works cross-functionally with sourcing, operations, and quality teams to support new product development and strategic supplier selection while driving continuous improvement in the supply base.
The Quality Engineer (Electronics) will oversee and improve manufacturing and quality processes by interfacing directly with production, resolving internal and customer issues through root cause analysis, and ensuring compliance with AS9100 and AS9102 standards. They will develop quality plans, conduct audits, manage supplier quality interactions, and drive continuous improvement initiatives within a high-reliability aerospace/defense environment.
This role oversees quality performance, employee supervision, and process compliance for high-precision aerospace manufacturing, ensuring products meet exacting tolerances and customer expectations. It combines hands-on employee coaching with supplier management, corrective action implementation, and continuous improvement leadership.
Seeking an experienced Quality Assurance Manager to oversee all production processes, ensuring products meet internal and external standards while leading a team of inspectors and technicians. This role focuses on maintaining operational excellence, proactively identifying quality issues, and supporting long-term business success.
This role oversees quality system compliance and process development for high-precision medical device manufacturing, ensuring adherence to ISO 13485 and 21 CFR standards. It combines hands-on production floor support with advanced quality engineering techniques like CAPA management, process validation, and continuous improvement initiatives.
As a Quality Engineer, you will manage and improve product and process quality within your Value Stream by performing statistical analyses, conducting audits, driving root cause investigations, and implementing continuous improvement initiatives. You will collaborate with suppliers, customers, and cross-functional teams to ensure compliance with quality standards and support the development of robust quality systems.
The Quality Engineer position involves ensuring compliance with FDA regulations and ISO 13485 standards, leveraging a minimum of 1-3 years of experience in medical device quality engineering. The role requires the ability to work cross functionally across many teams on the floor. Being able to wear many hats and work on several projects across not only Quality, but also R&D, Design and Manufacturing is essential for this position.
The Senior Quality Engineer plays a pivotal role within the quality team, ensuring that products and processes align with the client's Quality Management System (QMS). This position works closely with high-profile customers to investigate and determine the root causes of non-conformances, while partnering internally to develop and implement systems that drive quality improvements at the source.
The Quality Engineer will manage quality operations within the assigned Value Stream, ensuring adherence to product and process standards. They will gather statistical data for quality improvement, conduct root cause analysis, and guide technical evaluations to achieve plant quality objectives at our Reading, MA facility.
In this role, you will develop and maintain quality systems and procedures, including inspection plans and statistical analyses, to ensure product and process standards are met. Additionally, you will collaborate with cross-functional teams to address quality issues and drive continuous improvement initiatives.
This is a sanitation manager position with a client of ours in the food manufacturing space. Located in the Des Plains area, they are looking to bring on a Sanitation Manager to be hands-n, lead HAACP implementation, GMP, and general quality practices.
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