Engineer jobs in Middlesex

My client is seeking a Quality Engineer to support product quality, compliance, and process excellence at a leading medical device manufacturer. This role is ideal for someone who thrives in a hands‑on, regulated environment and enjoys driving root‑cause problem solving, validations, and continuous improvement.

The Design Quality Engineer leads design assurance and quality activities across the product lifecycle to ensure compliance with FDA, ISO 13485, and EU MDR requirements for Class III medical devices. This role supports NPI efforts, provides technical guidance to engineering teams, and drives high standards in risk management, validation, and supplier quality.

The position leads design assurance activities for new product development, ensuring full compliance with FDA, ISO, and global medical device regulations. It drives quality engineering efforts across the product lifecycle, including risk management, verification/validation, and process validation, while supporting cross‑functional teams and suppliers.

The Senior Supplier Quality Engineer will play a critical role in ensuring supplier quality within the engineering and manufacturing department. This position requires a proactive approach to quality assurance and collaboration with suppliers in the business services industry.

The Manufacturing Engineer will be a key hire for 2026 as they continue to grow their capabilities and hit record revenue numbers. They have a great leadership team in place with stability and room for growth.

The Manufacturing Engineer focuses on developing and optimizing processes to support high-volume, high-quality production in a cleanroom setting.

You will lead process standardization, equipment procurement, and continuous improvement initiatives while collaborating with global teams.

The Principal Mechanical Engineer will serve as the technical lead for the design, analysis, and development of their commercial systems. In this role you will collaborate with a cross-functional engineering team and external partners to bring both pilot-scale and commercial systems to life.

The Product Development Engineer will drive the design and development of advanced catheter products, ensuring performance, manufacturability, and regulatory compliance. This role focuses on delivering innovative solutions that support rapid growth and improve patient outcomes.

This role serves as the technical authority for the mechanical and structural design of commercial membrane-based process systems. The position leads design, analysis, fabrication oversight, and site integration in a fast-paced environment.

The Spinal Implant Instruments Development Engineer will play a key role in designing and developing innovative spinal implant instruments within the medical industry. This position requires expertise in engineering and manufacturing, with a focus on delivering high-quality solutions.

The Senior Extrusion Manufacturing Engineer will play a key role in optimizing manufacturing processes and ensuring high-quality product output. This role requires a strong technical background and a focus on process improvement and extrusion.

The Design Quality Engineer will play a critical role in ensuring the quality and compliance of medical device designs within the life science industry. This position involves working closely with engineering and manufacturing teams to uphold product quality and regulatory standards.

The Senior Mechanical Engineer will play a critical role in designing, analyzing, and implementing innovative mechanical systems and solutions for diverse projects. This position requires a strong engineering background, including expertise in complex piping systems, and a commitment to delivering high-quality, reliable results.

We are seeking a motivated Development Engineer to join a medical device organization. The ideal candidate will be responsible for developing and implementing engineering solutions to meet our project requirements, with a particular focus on applications related to medical device implants. This role involves designing and optimizing components that meet stringent regulatory standards and supporting innovation in implantable technologies.

The Development Engineer focuses on the full lifecycle development of surgical instruments supporting spinal implant systems. The role involves design, customization, regulatory compliance, and close collaboration with surgeons and implant design teams to deliver innovative, ergonomic solutions for complex procedures.

The position leads design assurance activities for new product development, ensuring full compliance with FDA, ISO, and global medical device regulations. It drives quality engineering efforts across the product lifecycle, including risk management, verification/validation, and process validation, while supporting cross‑functional teams and suppliers.

My client is seeking a skilled Principal Mechanical Engineer to lead and contribute to innovative engineering projects. This role requires strong technical expertise and a passion for driving excellence in engineering and manufacturing processes.

The Senior Manufacturing Engineer will play a pivotal role in optimizing production processes and ensuring efficient operations within the Engineering & Manufacturing department. This position focuses on driving continuous improvement initiatives, enhancing product quality, and supporting advanced manufacturing techniques such as extrusions for medical device applications.

The Quality Engineer will be responsible for ensuring compliance with medical device standards, driving root cause analysis, corrective actions, and continuous improvement through statistical and risk management practices. The position involves supporting validations, environmental monitoring, and quality system reporting to uphold product reliability and regulatory requirements.

My client is seeking a Quality Engineer to support product quality, compliance, and process excellence at a leading medical device manufacturer. This role is ideal for someone who thrives in a hands‑on, regulated environment and enjoys driving root‑cause problem solving, validations, and continuous improvement.

This Product Development Engineer leads the design and development of instruments from concept through commercialization, ensuring meeting with industry standards. It involves close collaboration with the medical industry, cross-functional teams, and design engineers to deliver effective solutions.

The Supplier Quality Engineer role focuses on ensuring supplier compliance and driving quality improvements across the supply chain by conducting audits, managing corrective actions, and supporting new product development. It requires collaboration with internal teams and suppliers to maintain standards, reduce risks, and implement continuous improvement initiatives.

This role ensures that external suppliers consistently meet stringent quality, regulatory, and reliability requirements for complex medical devices. It involves leading supplier audits, driving corrective actions, and partnering closely with engineering and manufacturing to prevent issues before they reach patients.