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The CNC Programmer will be responsible for developing and optimizing CNC programs to support manufacturing operations in the industrial and manufacturing sector. This temporary role requires expertise in precision machining and a commitment to ensuring high-quality production in Addison.
The multi-site Quality Manager plays a key role in enhancing and standardizing quality across multiple global manufacturing sites, promoting consistency and ongoing improvement. This position provides the chance to collaborate with senior leadership, lead cross-functional teams, and set the benchmark for quality excellence.
We are seeking a Design Quality Engineer to join a medical device/regulated‑industry team. In this role, you will help ensure that products meet safety, regulatory, and business requirements throughout the design lifecycle. You will work closely with cross‑functional teams on both new product development and sustaining projects of complex electromechanical systems (with software and disposables).
Quality Manager will play a critical role in ensuring the quality and efficiency of engineering and manufacturing processes within the business services industry. This permanent role in Boston offers an exciting opportunity for professionals passionate about quality management and operational excellence.
The Mechanical Engineer will support the design, development, and analysis of HVAC-related mechanical components and equipment. This position plays a key role in ensuring that products are designed, built, and delivered accurately and efficiently. The role involves working closely with the engineering and manufacturing teams to develop new designs, enhance existing products, and troubleshoot technical issues.
The Quality Engineer will lead and support quality assurance efforts within a manufacturing environment, including the development of quality standards, execution of internal audits, and resolution of quality issues through root cause analysis and continuous improvement initiatives. This role will also collaborate cross-functionally to monitor process performance, support external audits, and drive operational excellence in line with ISO 9001 standards.
Our client is seeking an experienced Quality Engineer or Senior Quality Engineer (depending on background) to join their growing quality department. This facility is currently ISO 9001 certified and is working toward achieving IATF 16949 certification. The ideal candidate will have a strong foundation in ISO quality systems, while prior experience with IATF standards and silicone-based products will be considered a significant advantage.
The Project Engineer will take ownership of leading, managing, and executing new product development (NPD) and manufacturing transfer projects within a regulated medical device environment. This role ensures that all initiatives are completed on time, within budget, and in compliance with FDA and ISO 13485 standards. It combines strategic project leadership with hands-on engineering execution and cross-functional collaboration.
The Project Engineer/Manager leads and manages medical device product development and manufacturing transfer projects from concept through production. The position combines hands-on engineering design, regulatory compliance, and project management to deliver high-quality products in a fast-paced, startup-like environment.
The Project Manager role supports the end-to-end development and manufacturing of medical devices in a highly regulated environment.The position blends project leadership, hands-on engineering, and compliance to drive successful product launches and process improvements.
Lead process development, validation, and continuous improvement initiatives for blow molding, injection molding, and assembly operations. Develop and optimize molding parameters for new and existing products to improve quality, cycle time, and efficiency.
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