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The Supplier Quality Engineer is responsible for enhancing the quality performance of the company's global supply base. This role involves conducting supplier audits, managing nonconformances, driving corrective actions, and ensuring that suppliers meet required standards from the outset of new product development.
You will enhance and maintain the Quality Management System by leading corrective actions, audits, supplier oversight, risk analysis, and process improvements. The role involves tracking quality metrics, supporting cross-team risk assessments, and ensuring adherence to key regulatory standards.
The Electronics Lab Automation Engineer will design, implement, and maintain automated lab systems for testing space-grade electronics. This includes creating software for controlling lab equipment, assembling test setups for off-site radiation testing, and ensuring precise, repeatable measurements. The role requires collaboration across engineering teams and occasional travel to off-site test facilities.
The Senior Laser Process Development Engineer will be a key member of the Manufacturing Engineering team, developing and optimizing laser-based processes for product development, packaging improvements, and high-volume production. This role involves troubleshooting laser systems, analyzing performance, improving efficiency, and collaborating across functions to achieve operational excellence.
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 Quality Engineer role focuses on hands-on support for manufacturing engineering, addressing non-conformances, implementing CAPAs, managing supplier quality, conducting audits, and executing QMS processes.
This Senior Quality Systems Engineer role focuses on managing and improving Quality Management System (QMS) processes, including CAPA, internal audits, and quality metrics, within a fast-paced medical device environment. The ideal candidate will ensure regulatory compliance, lead risk management initiatives, and drive continuous quality improvements across the organization.
As the Sr QE you will maintain and enhance the Quality Management System-managing document control, driving CAPA investigations through root cause analysis and verification of effectiveness, and supporting both internal and external audits. You will also analyze quality performance metrics, collaborate across teams to address non-conformances and supplier issues, and lead process improvement initiatives to ensure compliance with ISO 13485.
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