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Our client is a medical device manufacturer located in the Northern Suburbs of Chicago. With over 15 locations throughout the US and 5000 employees, they have continued to grow out new product lines. They seek a Quality Engineer to join their Quality team and oversee 3 production lines.
The Manufacturing Engineer will lead LEAN/Continuous Improvement initiatives for my client's fast-growing facility based in the NW suburbs of Illinois. You'll serve as the key player in efficiency improvement & cost savings, while also playing an exciting role in the future expansion of the business!
Our client, a leading medical device manufacturer based in the northern suburbs of Chicago, operates more than 15 facilities across the U.S. and employs over 5,000 people. Continuing to expand with new product lines, they are seeking a Quality Manager to join their Quality team and take responsibility for overseeing the department.
This is a Sr Quality Engineering opportunity with a manufacturer of various components used in high-profile medical devices. In this role, the Senior Quality Engineer will be responsible for managing customer communications, driving root cause analysis and corrective actions, and leading floor-level initiatives aimed at improving efficiency and operational performance.
The Mazak 5 Axis Programmer will play a key role in programming, setting up, and operating CNC machines to produce high-quality components. This position requires expertise in working with Mazak 5 Axis machinery and a strong understanding of industrial and manufacturing processes.
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
Are you an EHS professional with 2+ years of experience ideally in the Medical Device Manufacturing industry? Do you have a Degree related to Safety, Environmental, Chemical, or Engineering? Do you have strong understanding of OSHA and EPA regulations? If so, please read on and apply to the EHS Specialist - Medical Device Manufacturing job based in Danbury, CT.
Our client is a manufacturer of metal machined components serving the medical device industry. Their product is used in critical devices and quality is at the forefront of everythingn they do. With their developed team, they are looking for a senior level quality engineer to lead both internal and external projects.
Our client is a well-established medical device manufacturer headquartered in the northern suburbs of Chicago. With more than 15 facilities nationwide and a workforce of over 5,000 employees, they continue to grow through the launch of new product lines. To support this expansion, they are looking for a Senior Quality Engineer to join the Quality team and lead quality oversight for three production lines.
The Facilities Manager will oversee the maintenance and efficient operation of a multi-site manufacturing facility, ensuring compliance, safety, and reliability. The Facilities Manager leads a team and manages vendor relationships while driving long-term strategies for equipment and infrastructure.
The Project Engineer leads efforts in medical device development and manufacturing, making sure projects meet quality, budget, and timeline goals. This role involves both hands-on design work and project management skills in a regulated environment.
As a Senior Program Manager in the life science industry, you will oversee complex projects within the engineering and manufacturing department, ensuring their successful execution from initiation to completion. This role requires strong leadership and organizational skills to manage cross-functional teams.
The Facilities Manager will oversee the efficient operation, maintenance, and safety of facilities in the medical device industry. This role requires expertise in engineering and manufacturing processes to ensure optimal functionality and compliance while being able to manage a solid team of supervisors.
The CNC Swiss Lathe Programmer is responsible for interpreting a drawing and specifying the process, program and tooling required for production. Once blueprints are finalized and approved by management, the Programmer will set up the machines for production. The CNC Swiss Lathe Programmer is also responsible for leading the team of Machinists that will keep parts running without consultation to deliver low error, on-time results to the customer.
The Project Manager is a key contributor in driving medical device manufacturing and product development projects from concept to completion. In this role you will provide hands-on support for designs of components, evaluate processes and tooling, ensure accurate process documentation, and strengthen project execution.
The Project Manager role supports the end-to-end development and manufacturing of medical devices in a highly regulated environment.The position blends project leadership, hands-on engineering, and compliance to drive successful product launches and process improvements.
Our client is a leading medical device manufacturer headquartered in the northern suburbs of Chicago, with more than 15 facilities nationwide and a workforce exceeding 5,000 employees. As the company continues to grow and introduce new product lines, they are seeking a Senior Quality Engineer to join their Quality team and oversee three key production lines.
Ensure compliance with cGMP and maintain a safe, clean, and organized work environment. Keep detailed logs of tasks performed and communicate issues to supervisors.
The Quality Engineer will be responsible for ensuring compliance with quality standards and regulations within the medical device industry. This role will involve quality assurance, process improvement, and collaboration with cross-functional teams to drive excellence in product development and manufacturing.
Our client, a prominent medical device manufacturer located in the northern suburbs of Chicago, operates over 15 facilities nationwide and employs more than 5,000 people. As the company continues to grow with new product lines, they are seeking a Senior Quality Engineer to join their Quality team and oversee three dedicated production lines.
The Quality Engineer (Medical Device) will ensure that all products and processes meet established medical device quality standards by overseeing supplier quality, conducting validations, and implementing corrective actions for injection molded and purchased components. They will also develop and maintain quality control systems to support the full product lifecycle in a clean room manufacturing environment.
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