Medical Devices jobs

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.

This role supports manufacturing operations by ensuring strict adherence to quality system, regulatory, and documentation requirements for highly regulated products while monitoring production for compliance and product integrity. It also leads validations, risk analyses, CAPA activities, and continuous‑improvement initiatives while partnering cross‑functionally to strengthen processes and resolve quality issues.

The Engineering Manager will be a key hire to manage processes from beginning design phases all the way through production efforts. They will be a leader on the team to develop a smooth processes and life cycle of all products across Class I, II and III.

Lead and inspire a team of Product Life Cycle Engineers while driving cutting‑edge testing, compliance, and design improvements that keep advanced Class I-III medical devices at the forefront of global standards. As a cross‑functional force‑multiplier, you'll shape product strategy, elevate quality, fuel innovation, and ensure every device delivers exceptional performance and unmistakable customer value.

This Automation Engineering Manager works on managing the design and development of automated manufacturing equipment and processes from concept to production.

It involves leading engineering initiatives, mentoring team members, and driving continuous improvement in performance, safety, and cost.

My client is seeking a skilled and detail‑oriented Depot Service Engineer to support the repair, maintenance, and technical evaluation of advanced equipment used in fertility treatment technology and fertility laboratories. This role is based within a centralized service facility and focuses on diagnosing, repairing, testing, and refurbishing medical devices and laboratory technologies that support critical reproductive workflows.

A new product line is entering development, and my client needs a Quality Manager to guide its design activities and ensure compliance throughout the process. This position will also take the lead in creating and organizing documentation for the company's quality systems and related programs. The employer is a specialized manufacturer that builds electro-mechanical solutions exclusively for the medical device industry

The Project Engineer is a key leader in managing and executing medical device manufacturing and product development initiatives. This role ensures projects are delivered on time, within scope, and in compliance with FDA Quality System Regulations and ISO 13485 standards, while driving innovation and efficiency.

This is a senior-level Quality Engineering role with a medical device manufacturer located near the Illinois-Wisconsin border. The position is responsible for leading and supporting all quality assurance and quality control activities within a metal fabrication manufacturing environment.

This is a senior-level Quality Engineering role with a medical device manufacturer located near the Illinois-Wisconsin border. The position is responsible for leading and supporting all quality assurance and quality control activities within a metal fabrication manufacturing environment.

This role supports manufacturing operations by ensuring strict adherence to quality system, regulatory, and documentation requirements for highly regulated products while monitoring production for compliance and product integrity. It also leads validations, risk analyses, CAPA activities, and continuous‑improvement initiatives while partnering cross‑functionally to strengthen processes and resolve quality issues.

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.

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 position is responsible for managing quality systems, including audits, compliance with regulatory standards, and oversight of product release and corrective actions. The role requires strong leadership, regulatory knowledge, and experience in a highly regulated manufacturing environment.

You will lead the charge in developing smart, scalable, and compliant manufacturing methods that keep our medical devices at the highest standards. This role guides a team of technical experts and drives major initiatives-from production scale‑up to high‑volume manufacturing-that are essential to our growth and product excellence.

My client is a global industrial manufacturer for the automotive, aerospace, and medical device industries and is looking for a Senior Quality Engineer to join their growing quality department. The Senior Quality Engineer will be a leader on the team and will assist Quality Management with leading key continuous improvement quality projects and conducting internal and customer audits.

My client is a global industrial manufacturer for the automotive, aerospace, and medical device industries and is looking for a Senior Quality Engineer to join their growing quality department. The Senior Quality Engineer will be a leader on the team and will assist Quality Management with leading key continuous improvement quality projects and conducting internal and customer audits.

This opportunity is an operations manager position with a metal fabrication company that specifically servies the top medical device OEM customers in the industry.

This is a quality engineering opportunity with a medical device manufacturer that specializes in metal fabrication and CNC processes in particular. They are looking to add to their quality team to help support all QA/QC activity. Join a growing company at the forefront of their industry!

This role supports a premier life sciences transactions practice advising companies on structuring and executing deals across pharmaceuticals, biologics, medical devices, and digital health. The position offers exposure to sophisticated IP‑driven transactions and collaboration with multidisciplinary, cross‑office teams.

This role leads all site-level quality functions for a confidential medical device manufacturer operating in a highly regulated environment. The Senior Quality Manager drives compliance, audit readiness, and a culture of right‑first‑time execution while partnering closely with site and global leadership.

We are seeking a Quality Engineer specializing in CNC and medical devices to join a team in the business services industry. The ideal candidate will focus on ensuring product quality and compliance with industry standards while supporting continuous improvement initiatives.

This is a quality engineering opportunity with a medical device manufacturer that specializes in metal fabrication and CNC processes in particular. They are looking to add to their quality team to help support all QA/QC activity.

You will lead medical device development and manufacturing transfer projects from concept to production. This role combines hands-on engineering with project management to ensure timely delivery and regulatory compliance.

We are seeking a Quality Engineer specializing in CNC and medical devices to join a team in the business services industry. The ideal candidate will focus on ensuring product quality and compliance with industry standards while supporting continuous improvement initiatives.

The Project Engineer will manage new product development and manufacturing transfer projects for medical devices, ensuring compliance with FDA and ISO standards.

This role combines hands-on design work with leadership responsibilities across engineering, quality, and production.

We are seeking a dedicated Clinical Affairs Specialist to join our team in Irvine. The ideal candidate will play a key role in ensuring compliance with clinical regulatory requirements and supporting product development in the medical device manufacturing industry.

The Inside Sales Manager will lead and manage sales strategies within the Medical Device and Medical Manufacturing space. This role will be a player-coach position, working with your team and hitting your own sales goals.

This is a high-level Quality Engineering role with a medical device manufacturer located near the Illinois-Wisconsin border. The position is responsible for overseeing all QA/QC activities within a metal fabrication environment.