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Quality Engineer:This Quality Engineer role focuses on ensuring product and process compliance with medical device regulations by conducting risk assessments, supporting audits, and driving continuous improvement initiatives. The position involves cross-functional collaboration, quality documentation, and active participation in new product development to maintain safety, efficacy, and regulatory standards.
The Senior Manufacturing Engineer will wear many hats and support a small manufacturing environment. In this role you will get to work autonomously, supporting the manufacturing of new and existing surgical medical devices.
Are you a Quality Supervisor who has at least 3 years of experience working as a Quality Control Inspector? Do you have experience working with ISO 13485 and ISO 9001? Do you have a Metrology and/or CNC Programmer background? Do you have a strong understanding of First Article Inspections (FAI's)? If so, please read on and apply to the Quality Supervisor - Medical Device Manufacturing job based near Philadelphia, PA.
The Project Engineer will be a key leader in the execution of medical device manufacturing and product development projects, ensuring delivery within scope, on time, and in alignment with company goals. In this role you will be customer facing, communicating with them directly to ensure that projects are moving along smoothly.
As a Quality Engineer, you will play a key role in enhancing the quality of products and processes within an organization that values and prioritizes doing the right thing. This position offers the opportunity to support and guide adherence to established processes and procedures, ensuring the safety, effectiveness, and quality of products, as well as compliance with relevant standards and regulatory requirements.
The Manufacturing Engineer will be responsible to lead all manufacturing efforts onsite. You will support the new Manufacturing Engineering Leader.
The Quality Engineer is responsible for establishing, maintaining, and improving quality systems and processes-conducting audits, inspections, and statistical analyses to ensure products meet ISO/FDA standards and customer requirements. You will lead RCI's, drive corrective and preventive actions, collaborate with suppliers and internal teams, and support new product introductions through documentation, training, and continuous improvement efforts.
A hands-on manufacturing company seeking an experienced Manufacturing Engineer that will vital in supporting production through a variety of factos like process development, fixture design and assembly documentation. This role will also include collaboration across team and maintaining compliance in a fast-paced environment.
The Manufacturing Engineer will sit on a small team reporting into the Manufacturing Engineering Manager. In this role you will get to work autonomously, wearing many hats, supporting the manufacturing of surgical medical devices.
The Operations Manager will oversee daily production and technical operations, ensuring efficiency and quality. They will collaborate with cross-functional teams to drive process improvements and manage new product introductions.
We're hiring a Digital Marketing Manager to lead website strategy, performance marketing, SEO, and eCommerce growth for a mission-driven healthcare company.This is a hands-on role perfect for someone who loves the mechanics of modern marketing-connecting front-end UX with backend analytics, and turning clicks into conversions.
Do you have 3+ years of digital / content marketing experience? Are seeking a hybrid content marketing opportunity on the north shore of Boston, MA?
Do you have 7+ years of digital marketing & 2+ years of leadership / management experience within the medical device industry? Are seeking a remote marketing director role with where you can drive digital marketing campaigns?
Are you a medical device marketing digital specialist? Are you located on the north shore and looking for an excellent growth opportunity?
Are you a medical device marketing content specialist? Are you located on the north shore and looking for an excellent growth opportunity?
Are you a medical device marketing leader? Are you located on the north shore and looking for an excellent growth opportunity.
The Quality Engineer (Medical Device) will lead quality initiatives in a highly regulated, precision manufacturing environment, ensuring compliance with ISO 13485 and FDA 21 CFR Part 820 while driving continuous improvement across processes and systems. This position offers a clear path to advancement, and offers outstanding development opportunites.
My client is seeking a highly skilled Quality Manager to oversee day-to-day operations in their Buffalo, NY site. This site has three specific product lines and has just undertaken a new customer which has further increased performance. The role will have 10 direct reports and sit on the leadership team for the plant.
The Quality Engineer (medical device manufacturing) plays a key role in ensuring product and process quality through all phases of development, validation, and production, in compliance with ISO 13485 and FDA regulations. This individual will lead root cause investigations, support design controls, and drive continuous improvement initiatives in a fast-paced, innovation-focused environment.
My client is seeking the Quality Manager will lead a dynamic team in a growing medical technology facility, overseeing all quality systems and ensuring compliance with FDA and ISO-13485 standards. This role combines strategic leadership and hands-on management to drive continuous improvement, support regulatory readiness, and foster a culture of operational excellence at the Buffalo, NY facility.
As the Quality Engineer you will gain hands on experience in medical device development, focusing on manual testing, design controls, sterilization, and transit testing. You will collaborate closely with mechanical engineers and cross functional teams to ensure compliance with FDA regulations and ISO 13485 standards.
The Quality Manager (Medical Devices) will lead a dynamic team in a growing medical technology facility, overseeing all quality systems and ensuring compliance with FDA and ISO-13485 standards. This role combines strategic leadership and hands-on management to drive continuous improvement, support regulatory readiness, and foster a culture of operational excellence at the Buffalo, NY facility.
The Senior Advanced Manufacturing Engineer will work on a team that supports the development of new medical devices and improvements on exciting products. In this role, you will work on a variety of engineering tasks including working on product designs, managing complex projects, developing validation protocols and test methods, and working on continuous improvement initiatives.
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