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The Project Manager will oversee commercial interior construction projects from preconstruction through closeout, ensuring projects are delivered on time, within budget, and to the highest quality standards. This role requires hands-on experience with union contractors and close collaboration with estimating, design, and field teams during preconstruction.
This role drives quality throughout design and development, ensuring compliance and product excellence. You will partner with engineering teams to embed robust quality practices while supporting regulatory and risk management activities.
This position plays a key role in ensuring product quality and regulatory compliance across the full lifecycle of advanced medical devices. You will collaborate cross-functionally to drive continuous improvement, streamline processes, and uphold the highest standards of excellence in manufacturing and design.
A civil construction superintendent specializing in heavy highway projects oversees day-to-day field operations for large-scale infrastructure work such as highways, bridges, and interchanges, ensuring projects are built safely, on schedule, and within budget. They coordinate crews, subcontractors, equipment, and inspectors while maintaining strict compliance with DOT standards, quality requirements, and site safety regulations.
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 Senior Design Quality Engineer is responsible for ensuring quality is embedded throughout the product development lifecycle, from concept through commercialization and post-market support. This role partners closely with cross-functional teams to ensure products meet regulatory requirements, internal quality standards, and customer expectations.
The Senior Quality Engineer is responsible for leading and maintaining processes across the product lifecycle in compliance with applicable regulatory standards and internal quality requirements. This role ensures that product risks are systematically identified, evaluated, mitigated, and monitored, supporting the development and commercialization of their product line.
This role is a hands-on Quality Engineer position focused on strengthening the QMS, supporting production, and executing facility transfer initiatives in a regulated medical device environment. You will play a critical role in ensuring compliance, driving CAPA and root cause investigations, and maintaining high-quality output during operational transitions.
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