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The Supplier Quality Engineer role focuses on ensuring supplier compliance and driving quality improvements across the supply chain by conducting audits, managing corrective actions, and supporting new product development. It requires collaboration with internal teams and suppliers to maintain standards, reduce risks, and implement continuous improvement initiatives.
The Design Quality Engineer ensures that all medical device design and development activities meet safety, performance, and regulatory standards. This role partners with cross-functional teams to support new product development and sustaining engineering projects, driving quality, compliance, and risk management throughout the design lifecycle
This role ensures that external suppliers consistently meet stringent quality, regulatory, and reliability requirements for complex medical devices. It involves leading supplier audits, driving corrective actions, and partnering closely with engineering and manufacturing to prevent issues before they reach patients.
The quality engineer will help lead all quality-driven activity associated with the design and manufacturing of precision medical devices and components. The ideal candidate will help lead all audits, handle QA/QC activity, and work cross-functionally with engineering teams to ensure product and customer standards are met.
The role oversees quality systems by leading customer complaint investigations, managing audits, and maintaining compliance with multiple industry standards. It also manages document control, calibration processes, and cross‑functional quality improvements while supporting external quality system interactions.
We are seeking a motivated Development Engineer to join a medical device organization. The ideal candidate will be responsible for developing and implementing engineering solutions to meet our project requirements, with a particular focus on applications related to medical device implants. This role involves designing and optimizing components that meet stringent regulatory standards and supporting innovation in implantable technologies.
This Product Development Engineer leads the design and development of instruments from concept through commercialization, ensuring meeting with industry standards. It involves close collaboration with the medical industry, cross-functional teams, and design engineers to deliver effective solutions.
This is a high level quality engineering position with a medical device manufacturer near the IL/WI Border. This role will engage in all QA/QC activity in metal fabrication environment.
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