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This is a highly autonomous Quality Engineer role where you'll lead US regulatory and quality oversight for FDA‑cleared implantable medical devices manufactured overseas. You'll act as the primary FDA liaison while building and maintaining a compliant, inspection‑ready quality system across international partners.
The Product Engineer will play a key role in designing and developing innovative spinal implant devices within the medical industry. This position requires collaboration with surgeons in medical environments and using engineering expertise with a focus on delivering high-quality solutions.
The Spinal Implant Instruments Development Engineer will play a key role in designing and developing innovative spinal implant instruments within the medical industry. This position requires expertise in engineering and manufacturing, with a focus on delivering high-quality solutions.
This role serves as the U.S. quality and regulatory owner for FDA‑cleared implantable medical devices manufactured overseas. You'll lead QMS execution, design controls, supplier quality, and regulatory compliance while working closely with global partners.
The Senior Quality Engineer will be responsible for supporting new product development in a regulated environment, with responsibility for design controls, risk management, quality systems, and regulatory compliance. Partners with engineering teams to ensure products are developed, validated, and commercialized in accordance with FDA, ISO, and global quality standards in Mount Laurel, NJ.
This Senior Quality Engineer role owns quality system compliance, customer quality issues, and corrective action activities within a regulated manufacturing environment. The position is customer‑facing and heavily involved in audits, MRB, and continuous improvement tied to AS9100 requirements.
The Manufacturing Engineer supports new product development and transitions designs into production-ready processes. This role partners with engineering, logistics, and production teams to improve manufacturability, troubleshoot issues, and support ongoing operations.
Our client is seeking a Quality Assurance Engineer to ensure their medical devices meet quality, performance, and regulatory requirements throughout design and manufacturing. The role involves quality systems, testing, audits, CAPA management, and collaboration with engineering and manufacturing teams
The Manufacturing Process Engineer will partner closely with design engineers, scientists, technicians, and production teams to ensure new products are designed for manufacturability and successfully transitioned into production. This individual will also play a key role in continuous improvement efforts, troubleshooting production issues, and supporting day‑to‑day manufacturing operations.
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