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The Development Engineer will be a key player in the development and design of catheters for some of the largest medical device and health-care organizations across the country.
The Quality Manager, medical device manufacturing, will lead the maintenance and continuous improvement of the quality management system to ensure compliance with regulatory standards and internal requirements at our Marlborough facility. They will oversee supplier quality, incoming inspection, and production support to drive consistency in product and process quality across the organization.
The Manufacturing Engineer is responsible for implementing lean processes, equipment, and tooling for new and redesigned products, focusing on improving manufacturing efficiency. They collaborate with the new product development team to drive cost reductions, improve processes, and minimize waste and rework.
Key responsibilities as an EHS manager include ensuring regulatory compliance, preventing accidents, conducting training, managing waste and hazardous materials, and acting as the primary point of contact for EHS audits. The position requires collaboration with management to integrate EHS policies into daily operations, track performance metrics, and drive continuous improvement towards safety and sustainability goals
My client is seeking a dedicated Senior Development Engineer who can blend creativity and technical expertise to bring to our organization. The ideal candidate will have a strong understanding of both hardware and software systems, and be proficient in design, testing, and debugging.
The Safety Manager is responsible for planning, directing, and managing all safety activities within a manufacturing environment, with a focus on promoting a strong safety culture. This role involves developing and implementing safety programs, conducting compliance audits, providing training, and ensuring adherence to regulatory requirements to minimize risks and maintain a safe workplace.
The Principal Lean Director, Manufacturing will serve as a hands-on subject matter expert and partner to site leadership, driving continuous improvement initiatives and embedding Lean principles across operations. They will collaborate globally to standardize best practices, foster a culture of operational excellence, and deliver measurable value to both internal and external customers at our Hopedale, MA facility.
This is a hands-on quality leadership role within a lean, collaborative manufacturing environment, responsible for driving both systems and operational quality. The position involves managing a small team, leading audits and compliance efforts, and partnering across departments to ensure product and process excellence in a regulated setting.
The Quality Engineer Manufacturing will lead root cause investigations, support continuous improvement initiatives, and ensure compliance with internal and external quality standards. They will collaborate cross-functionally to improve processes, enhance product quality, and maintain robust documentation within the Quality Management System.
The Quality Manager, medical device manufacturing, will ensure products meet strict quality standards while driving continuous improvement to enhance reliability and performance. This role focuses on optimizing operational efficiency and implementing technical solutions to deliver high-quality products on time at our Bedford, MA facility.
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