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The Quality Systems Engineer supports manufacturing and inspection of advanced aerospace components, ensuring compliance with AS9100 standards and customer requirements. The role involves managing audits, driving root cause investigations, and maintaining quality system documentation to support high-reliability production.
As the Reliability Engineer you will lead numerous reliability engineering projects in a fast-paced, cross-functional environment. You will also ensure proliferation of design for reliability methods into new product developments, plan the reliability validation tests, and lead the qualification of parts/assemblies in support of release.
The Quality Engineer ensures product quality and compliance by implementing and monitoring quality systems, conducting audits, and working on the production floor. They collaborate with cross-functional teams to improve processes, ensure regulatory compliance, and support continuous improvement initiatives.
The Reliability Engineer focuses on ensuring the dependability and performance of aerospace systems through analysis, testing, and failure investigations. The role involves collaborating with cross-functional teams to improve product designs, implement reliability standards, and optimize maintenance strategies for enhanced operational efficiency.
The production manager oversees daily operations in a small machine shop clean room, ensuring efficient workflow and adherence to quality standards. They coordinate with teams to maintain productivity while upholding safety and cleanliness protocols.
The Quality Engineer, medical device manufacturing, will work to improve the quality of products and processes while operating in a culture highly receptive to quality. You will have the opportunity to support and provide guidance to ensure adherence to processes and procedures that maintain safety, efficacy, and compliance with applicable standards and regulations onsite at out Hudson, NH facility.
Quality Engineer:This Quality Engineer role focuses on ensuring product and process compliance with medical device regulations by conducting risk assessments, supporting audits, and driving continuous improvement initiatives. The position involves cross-functional collaboration, quality documentation, and active participation in new product development to maintain safety, efficacy, and regulatory standards.
This is an excellent opportunity for a R&D with Non-Wovens specific experience to grow and develop in a hands-on capacity. This individual will be responsible for interfacing with customers, practicing creativity and must have experience working with new product development.
The newly created COO role will be crucial in the Development firm's expansion across the US.Historically our client have developed projects from inception through to NTP. They are now evolving to become an IPP where the focus will be utility-scale solar, storage and wind projects across PJM, MISO, SERC, ISO-NE- NY-ISO.
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