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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.
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 Senior Manager of Facilities is responsible for overseeing the planning, design, construction, and maintenance of all company facilities to ensure operational efficiency and compliance. This role provides strategic leadership for site development, space optimization, and new construction projects while managing budgets, contractors, and cross-functional collaboration.
The Director of Packaging Engineering will lead the development and execution of innovative packaging solutions for the personal care manufacturing industry. This position requires expertise in engineering and manufacturing, with a focus on delivering high-quality, sustainable, and cost-effective packaging solutions.
Our client, an innovative forging manufacturer serving the automotive industry, is seeking a Quality Engineer to join their expanding team. The ideal candidate will have experience with IATF 16949, PPAP, and customer complaint management.
The Quality Engineer will play a critical role in ensuring the organization maintains its reputation for excellence in precision manufacturing. This position will lead quality initiatives across production, drive continuous improvement, and ensure compliance with ISO/TS 16949 and customer-specific requirements.
This role is for a Controls Engineer with a manufacturing company near O'Hare. The position focuses on designing, developing, implementing, and maintaining electrical control systems in a metal manufacturing environment, ensuring automated equipment and production processes operate safely, reliably, and efficiently
The position leads design assurance activities for new product development, ensuring full compliance with FDA, ISO, and global medical device regulations. It drives quality engineering efforts across the product lifecycle, including risk management, verification/validation, and process validation, while supporting cross‑functional teams and suppliers.
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