Medical Devices jobs

This role leads R&D efforts for implantable biologic materials, supporting product development, test method creation, tech transfers, and early‑stage research. You'll design manufacturing steps, run analytical testing, and contribute to expanding the biologics portfolio.

This Director-level role oversees all Regulatory Affairs and Quality Assurance activities, ensuring the company meets global medical device standards while expanding its product portfolio. You will shape regulatory strategy, strengthen the QMS, and drive compliance across a highly innovative environment.

We are seeking a highly experienced Principal Engineer with a strong background in medical device engineering to lead critical initiatives across both new product development (NPD) and post‑market sustaining engineering. This role will play a key part in ensuring product performance, safety, compliance, and continuous improvement across a diverse portfolio of Class I, II, and III medical devices.

This role is ideal for an experienced engineer who thrives in a fast‑growing, innovation‑driven medical device environment. You will play a critical role in the development, optimization, and lifecycle management of implantable medical devices designed to improve outcomes for patients with chronic heart failure.

The Director, Site Engineering Leader will provide strategic and technical leadership across a high‑volume manufacturing site specializing in extrusion, injection molding, and highly complex automation systems. This individual will guide a multidisciplinary engineering organization, ensure continuity of 24/7 operations, and play a critical role in shaping the site's long‑term growth, capital planning, and operational excellence.

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.

This role leads engineering support for manufacturing operations, driving process improvements, resolving technical issues, and ensuring production quality and regulatory compliance. It also manages engineering projects, directs a team of engineers, and implements Lean and continuous‑improvement initiatives to optimize high‑volume medical device manufacturing.

You will lead the site's manufacturing engineering and automation agenda for a high‑volume, regulated production facility. Partnering closely with operations, you'll optimize complex extrusion, injection molding, and automated assembly lines to ensure safe, reliable supply of life‑sustaining products.

This role leads the full product life-cycle (defining market‑driven requirements, shaping long‑term portfolio strategy, executing product launches, supporting commercial teams) to drive growth in a life‑science organization. It requires strong technical, analytical, and leadership capabilities to partner cross-functionally, guide R&D, support sales, and ensure successful product performance in biopharma markets.

Seeking a hands-on leader to drive the Continuous Improvement program for Manufacturing Operations. This role serves as the Lean/CI expert-coaching teams, partnering with site leadership, and leading initiatives that improve manufacturing and back‑office processes. The position collaborates globally to advance Lean practices and requires strong leadership, problem‑solving skills, and deep knowledge of CI tools.

My client is seeking a Manufacturing Technician to be involved in hands‑on work building and inspecting components for minimally invasive implantable pulse generators and external programming systems.The ideal candidate is detail‑oriented, quality‑driven, and comfortable working in a regulated, high‑precision medical device production environment.

This role serves as the U.S.-based quality and regulatory lead, ensuring full compliance with medical‑device regulations while overseeing quality systems, supplier performance, and imported product controls. It supports audits, design transfer, CAPA, inspections, and end‑to‑end oversight of global manufacturing partners to maintain product safety, documentation accuracy, and regulatory readiness.

In this role, you will be instrumental in introducing, optimizing, and scaling processes for Nitinol tube and wire manufacturing, serving as a key technical liaison between Production, Quality, and Engineering. This is a hands‑on engineering position with real ownership of systems, processes, and improvements.

You will drive advanced manufacturing process development, CNC programming, and production readiness for medical device components and assemblies. This role supports both new product introduction (NPI) and ongoing manufacturing optimization for Class II and III devices-including CNC‑machined components, catheter subassemblies, and finished device manufacturing.

This role leads quality system compliance and process development for complex, highly regulated products, ensuring design controls, risk management, validations, and documentation all meet stringent industry and customer requirements. It drives product quality, CAPA activities, audits, and cross‑functional collaboration while mentoring junior engineers and supporting continuous improvement in a fast‑paced manufacturing environment.

This role leads all Regulatory Affairs and Quality Assurance activities, ensuring global compliance while supporting rapid growth and innovation. You'll partner closely with senior leadership to guide regulatory strategy across the full product lifecycle.

This role is ideal for an experienced engineer who thrives in a fast‑growing, innovation‑driven medical device environment. You will play a critical role in the development, optimization, and lifecycle management of implantable medical devices designed to improve outcomes for patients with chronic heart failure.

This Senior Quality Engineer role supports quality system compliance, process development, and validation within a fast‑paced, high‑tech medical device manufacturing environment. You will lead risk management, CAPA, supplier interactions, and documentation while collaborating cross‑functionally to ensure product safety and regulatory compliance.

My client is a global industrial manufacturer for the automotive, aerospace, and medical device industries and is looking for a Quality Engineer to join their growing quality department. The Quality Engineer will primarily responsible for process validation and production change management activities.

My client is a global industrial manufacturer for the automotive, aerospace, and medical device industries and is looking for a Quality Engineer to join their growing quality department. The Quality Engineer will primarily responsible for process validation and production change management activities.

This is an Assistant Quality Manager Role, reporting to the Director of Quality, for a plastics injection molding operation in the western suburbs of Chicago, specialized for automotive customers as well as medical device and industrial.

This Director-level role oversees all Regulatory Affairs and Quality Assurance activities, ensuring the company meets global medical device standards while expanding its product portfolio. You will shape regulatory strategy, strengthen the QMS, and drive compliance across a highly innovative environment.

The Operations Leader - Precision Manufacturing will oversee and enhance production processes, ensuring efficiency and quality in a high-tech manufacturing environment. This role is ideal for a professional with expertise in machining, production management, and leadership within industries such as aerospace, defense, and medical devices.

My client is a global industrial manufacturer for the automotive, aerospace, and medical device industries and is looking for a Quality Engineer to join their growing quality department. The Quality Engineer will primarily responsible for process validation and production change management activities.

My client is a global industrial manufacturer for the automotive, aerospace, and medical device industries and is looking for a Quality Engineer to join their growing quality department. The Quality Engineer will primarily responsible for process validation and production change management activities.

The position oversees tooling and mold design activities while ensuring new and existing products are optimized for manufacturability, cost efficiency, and high‑quality production. It requires deep expertise in mold design, DFM, and collaboration with global manufacturing partners, particularly within regulated or medical‑device environments.

We are seeking a Sales Account Manager specializing in injection molding to join a hybrid role in Nashua, NH area, providing top-tier service to the medical device market.

As a Senior Process Development Engineer, you will design, implement, and validate manufacturing processes for cutting‑edge implantable electronic medical devices. You'll lead engineering initiatives, improve production capabilities, and collaborate cross‑functionally to support next‑generation medical technologies in Mount Laurel, NJ.

The Senior Quality Engineer will play a crucial role in ensuring the quality and compliance of products within the medical device industry. This position is based near Stow, OH, and requires a detail-oriented professional with strong technical skills in quality assurance and manufacturing processes.

This a brand new on-site position for a leading medical device organization in Burlington, Massachusetts and the Senior SQL & Power Platform Developer will be responsible for designing, developing, and supporting scalable data and automation solutions that enable efficient business operations and informed decision-making. This role combines strong SQL Server expertise with hands-on experience in Microsoft Power Platform to deliver end-to-end solutions