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My client is seeking a Senior Mechanical Design Engineer to join a thriving team within the industrial metals manufacturing space. This role focuses on designing and developing innovative mechanical systems and components while ensuring quality standards are met.
A family owned general contractor based in the South Shore, MA is seeking a Project Engineer to join their team on a large scale Water Treament Plan. This is an Urgent Need - submit your resume today for immediate consideration.
Our client is seeking a Project Engineer with 1-2+ years of construction experience to join their Halifax office and support a $26M water treatment plant project in Plainville, MA. The Project Engineer will play a key role in both project execution and preconstruction efforts. This role is ideal for someone who is looking to learn, grow, and advance with a well-established and stable company.
As the Sr QE you will oversee product quality from start to finish-reviewing contracts and drawings, processing Engineering Change Orders (ECOs), and identifying both internal and external corrective actions to steer issues toward resolution. Much of your time is reactive "fire‑fighting," navigating diverse activities until each quality issue is closed.
My client is seeking a proactive and collaborative Process Engineer to join their Engineering team and support manufacturing operations and continuous improvement initiatives. This role is ideal for someone who enjoys working cross-functionally, solving complex problems, and contributing to a culture of safety, quality, and innovation. The Process Engineer will be instrumental in optimizing production processes and supporting engineering objectives across the facility.
As a Process Engineer, you'll play a key role in improving manufacturing processes, supporting production teams, and implementing technical solutions that enhance efficiency, quality, and safety. You'll work closely with cross-functional teams to troubleshoot issues, introduce new equipment, and drive continuous improvement initiatives.
The Quality Manager leads the company's Quality Systems in compliance with ISO 13485 and global medical device regulations, ensuring robust oversight of product release, CAPA, audits, and technical investigations. This role is critical in maintaining regulatory readiness and driving continuous improvement across the organization's quality operations.
The Quality Manager role is a hands-on position focused on maintaining and enhancing quality systems to meet AS9100 and MIL-spec standards. It offers autonomy, cross-functional collaboration, and the opportunity to grow professionally in a small, agile team environment.
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