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The Quality Engineer 3 position with my client involves ensuring adherence to quality standards and regulatory requirements in the production of medical devices and pharmaceutical products. Responsibilities include conducting quality assessments, implementing corrective actions, and collaborating cross-functionally to drive continuous improvement in product quality and reliability.
A Quality Engineer will be responsible for ensuring product quality by applying statistical analysis and quality control methodologies in precision manufacturing. This candidate will collaborate with cross-functional teams to address and prevent quality issues, emphasizing continuous improvement and adherence to high-quality standards.
The main role of a Manufacturing Engineer is to work collaboratively with customers and engineering teams to develop price quotations for components. This individual will create cost estimates, production time lead, and NRE/NRT estimates as well as support operations on the shop floor, tool design, and cycle time improvements.
The Electrical Systems Engineer will lead development efforts of the product system accessories. This is a hands-on position that will provide the opportunity for the right individual to build and manage a team.
The Process Engineer is responsible for establishing and improving process operations within the electronics manufacturing space. In this role, the Process Engineer will be working with chemicals, and equipment related to chemicals, and should be coming from a similiar background.
The Mechanical Engineer is responsible for managing the development and improvement of operations within the electronics manufacturing space. In this role, the Mechanical Engineer will work on design improvements for products and equipment.
The Manufacturing Engineer will be hands on in the production of several different product lines while incorporating new and innovative ways to develop more products for the future.
As the Chemical Engineer, you will be responsible for directly supporting chemical operations. You will make chemical adds and will transport samples to be analyzed at various locations.
As the Process Engineer, you will be responsible for the chemical process operations for this company. You will manage the setup of equipment and processes to ensure production efficiency.
As the Mechanical Engineer, you will assist with mechanical engineering activities within the operation. You will be a key player in improving equipment efficiency and installing new equipment.
Our client, a top rated General Contractor, is looking to bring on a project engineer. Apply today for immediate consideration!
The Engineering Manager will be responsible for leading the sustaining engineering department with 6 direct reports on-site in Marlborough, MA.
The role involves overseeing and leading the sustaining engineering department, with responsibilities ranging from creating process documentation to solving equipment maintenance issues in support of Manufacturing. Additionally, the position requires providing technical support for production coating processes, including tasks such as process development, root cause analysis, systematic problem-solving, and metrics management.
The Electrical Systems Engineer will spearhead the development of a class ll medical device and accompanying system accessories. This position entails hands-on involvement and offers the chance for the suitable candidate to establish and oversee a team.
The Manufacturing Engineer will be responsible for developing cost-effective die casting methods and optimizing machining and assembly processes. The candidate will lead the planning and execution of manufacturing processes, emphasizing efficiency, cost reduction, and collaborative teamwork across departments.
Your role as a Quality ambassador in the Specialty Products division is centered on boosting awareness, visibility, and communication regarding quality, with a particular focus on aligning these efforts with the division's unique needs and objectives.
As the Mechanical Engineer III, you will be responsible for leading the development of innovative products and accessories for the medical device space. You will design, build, and test new products from concept through to production.
The Senior Mechanical Engineer will lead the development of new and innovative products and accessories in the medical device space. This individual will also work to develop and improve processes in order to delivery the highest quality products for customers.
This Quality Engineer will have the chance to come in and immediately make a difference in multiple industries that our client supports. Work in a state of the art plant, utilizing skills such as SPC, Gage R&R, PPAPs, and GD&T to enhance product quality for numerous of our clients customers.
Quality activities, risk management activities, supplier qualifications, sustaining engineering, new product development, operational quality activity, equipment qualification, docu and design change control, QMS development, process development, design V&V as well
As the Mechanical Engineer II, you will be responsible for leading the development of innovative products and accessories for the medical device space. You will design, build, and test new products from concept through to production.
The Mechanical Engineer III will be focusing on developing and enhancing manufacturing processes. This role involves CAD design, testing, and iteration, while providing direction to technicians and external teams.
The Principal Systems Engineer will lead cross-functional efforts to implement aesthetic laser system projects, defining requirements and overseeing the development of system specifications. They will also conduct testing, document results, and generate final reports with a focus on subsystem interfaces and design verification.
The Mechanical Engineer lll will be a hands-on technical contributor, mainly focused on Class lll medical devices. In this role you will help lead the development of new products, working on design and testing of new devices.
The Senior Quality Engineer will enhance awareness, visibility, and communication regarding quality initiatives while supporting departmental, functional, and corporate quality goals within a medical device manufacturing space. The ideal candidate will possess a robust understanding of FDA/ISO 13485 Quality System requirements, GxP standards, and other pertinent regulations.
Step into the role of Senior Quality Assurance Specialist, where you'll leverage your extensive experience to ensure adherence to the highest quality standards and regulatory compliance within the dynamic field of medical devices. As a key player, you'll spearhead initiatives aimed at driving innovation and advancing patient care through meticulous attention to detail and a commitment to excellence.
The Forge Manufacturing Engineer will play a crucial role in ensuring the efficient and effective production of forged components used in medical devices. The ideal candidate will have a strong background in forge process development, materials science and quality assurance.
In this role you will be focused on ensuring the quality and regulatory compliance of product designs. Responsibilities may include overseeing design control processes, conducting risk assessments, and collaborating with cross-functional teams to develop and implement quality management systems.
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