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This position is part of a small, collaborative hardware and production group focused on building high‑performance connected products. You'll work across the full product lifecycle-supporting development builds, addressing issues surfaced during manufacturing and field use, and contributing to design improvements and cost‑reduction initiatives.
The Senior Quality Manager sets and executes the site's quality vision while ensuring products meet regulatory, customer, and compliance expectations. This role blends strategic leadership with hands‑on operational oversight to improve systems, build capability, and elevate performance.
You will join a collaborative hardware and production engineering group responsible for designing, building, validating, and supporting our products throughout their lifecycle. This position plays a key role in diagnosing electrical issues, improving system reliability, supporting global manufacturing, and contributing to next‑generation product development.
The role focuses on resolving electrical issues found in development, manufacturing, and the field, while contributing to design improvements, cost reduction efforts, and preparation for entry into the EU market. You will work closely with hardware, firmware, manufacturing, and supplier teams in the US and Asia to improve system reliability and performance.
This position oversees early‑stage manufacturing operations within a medical‑technology environment, focusing on prototype builds, validation efforts, and the initial phases of production. The role bridges engineering and operations, ensuring new products are assembled reliably through well‑designed processes, solid documentation practices, and disciplined execution before scaling into broader manufacturing.
As a Firmware Engineer, you will be responsible for designing, developing, and testing firmware solutions that contribute to the success of the Technology department. This role offers an exciting opportunity to work in the Business Services industry, leveraging your technical expertise to deliver innovative solutions.
This Director-level role oversees all Regulatory Affairs and Quality Assurance activities, ensuring the company meets global medical device standards while expanding its product portfolio. You will shape regulatory strategy, strengthen the QMS, and drive compliance across a highly innovative environment.
This role leads all regulatory affairs and quality assurance functions, ensuring global compliance and driving continuous improvement across the organization. You'll oversee submissions, audits, QMS strategy, and partner closely with executive leadership on regulatory direction.
This Senior Quality Engineer will own key quality systems, audits, and customer-facing problem resolution while ensuring ongoing compliance with AS9100D and ISO9001:2015. You'll be a trusted technical leader driving corrective actions, new product quality plans, and continuous improvement initiatives.
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