medical device Jobs

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Engineer Sr I - Product Improvement - Medical DevicesJob Title - Engineer Sr I - Product Improvement - Medical Devices

ArthrexCompany Name - Arthrex

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Goleta, California, USA

Full-time

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education. We are a privately held company that strives to accomplish our corporate mission of Helping Surgeons Treat Their Patients Better . We are committed to delivering uncompromising quality to the health care professionals who use our products, and ultimately, the millions of patients whose lives we impact. Arthrex Benefits Medical, Dental and Vision Insurance Company-Provided Life Insura

Electrical Engineer II (Instrumentation Support)Job Title - Electrical Engineer II (Instrumentation Support)

Autonomous Medical Devices IncorporatedCompany Name - Autonomous Medical Devices Incorporated

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Santa Ana, California, USA

Full-time

Autonomous Medical Devices Incorporated (AMDI), based in California, is a fast-growing company on a mission to transform point-of-care diagnostics. Our team of world-class engineers, scientists, clinicians, and manufacturing experts is pioneering breakthrough technologies in microfluidics, protein engineering, and cloud-connected data systems. We're gearing up to launch our inaugural products from our ISO 13485-certified, 110,000-square-foot facility in Santa Ana, CA - and we're looking for pass

Program Manager-Medical DeviceJob Title - Program Manager-Medical Device

Judge Group, Inc.Company Name - Judge Group, Inc.

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Marlborough, Massachusetts, USA

Contract

Location: Marlborough, MA Salary: $140,000.00 USD Annually - $165,000.00 USD Annually Description: Our client is currently seeking a Program Manager-Medical Device who will be responsible for managing large-scale, highly complex, multi-faceted new medical product development programs, involving internal and external development partners. Provides technical leadership in design, test and system integration of medical devices and instruments. Plans of all program subsystem and project deliver

Sr Engineer (Medical Devices)Job Title - Sr Engineer (Medical Devices)

Ledgent TechnologyCompany Name - Ledgent Technology

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Irvine, California, USA

Contract

We are seeking Medical Device Quality Engineering candidates to be considered for a Medical Device Quality Engineering position tha we have available in Irvine, CA. Knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and company systems / procedures to optimize product development, internal and external device manufacturing, and device distribution. This role is W2 hourly with Roth Staffing (Ledgent is a division of Roth). No 3rd party can

Junior Medical Devices Quality Associate (2 Openings)(ONSITE)(No C2C/H1B)Job Title - Junior Medical Devices Quality Associate (2 Openings)(ONSITE)(No C2C/H1B)

NetSource, Inc.Company Name - NetSource, Inc.

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Cedar Creek, Texas, USA

Contract

(No C2C/H1B) Please note that this is a 6 to 18-month contract position. Only local candidates need to apply. Notes: needs to have medical device or life science experience. Also should understand these compliance terms: Ensures compliance with relevant regulations and guidelines, ISO 13485, 21 CFR Paart 820, and IVDR. Qualifications Bachelor s degree required.1-2 years relevant quality experience in a manufacturing environment.1+ years of SAP experience.Focused on product release processes, en

Clinical Evaluation - Senior Project Manager - Medical Devices (on-site)Job Title - Clinical Evaluation - Senior Project Manager - Medical Devices (on-site)

Abbott LaboratoriesCompany Name - Abbott Laboratories

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Plano, Texas, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Yo

Program Manager- Medical DeviceJob Title - Program Manager- Medical Device

Judge Group, Inc.Company Name - Judge Group, Inc.

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Marlborough, Massachusetts, USA

Contract

Location: Marlborough, MA Salary: $150,000.00 USD Annually - $165,000.00 USD Annually Description: We are seeking a highly skilled Program Manager to lead the development of large-scale, complex medical device programs, working with both internal and external partners. This role provides technical leadership in design, testing, and system integration while ensuring compliance with industry standards and delivering projects efficiently and within budget. Key Responsibilities Oversee multi-fa

Mechanical Engineer- R&D, Medical DeviceJob Title - Mechanical Engineer- R&D, Medical Device

Eliassen GroupCompany Name - Eliassen Group

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Marlborough, Massachusetts, USA

Contract

Description: Our client is a privately held medical device that innovates in the area of atrial fibrillation. Their focus is dedicated to advancing innovative treatments while creating more accessibility to patients in need. They have recently acquired a world-leading organization and are working on the next generation of a cardiac ablation system. The company is positioned well for rapid growth, while also allowing employees to be a part of a purposeful mission in developing lifesaving technol

Sr. Firmware Engineer (Medical Device/Regulated industry)Job Title - Sr. Firmware Engineer (Medical Device/Regulated industry)

Oxford Global ResourcesCompany Name - Oxford Global Resources

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Santa Clarita, California, USA

Contract

Position Title: Sr. Firmware Engineer (Medical Device / Regulated Industry) Location: Valencia, CA Hybrid onsite Duration of Contract: 12+ Months (Minimum through April 1st, 2026; likely extension) Schedule: (9/80 schedule; every other Friday off) Interview Process: Resume ReviewInterview with the team (4 members of the team)Back-to-back 30-minute interviews (total duration: 2.5 hours) Scope of Work: Join a highly specialized team working on a next-generation medical device platform. You ll con

Junior Medical Devices Quality Associate (2 Openings)(ONSITE)(No C2C/H1B)Job Title - Junior Medical Devices Quality Associate (2 Openings)(ONSITE)(No C2C/H1B)

NetSource, Inc.Company Name - NetSource, Inc.

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Cedar Creek, Texas, USA

Contract

Manufacturing Quality Engineer (Medical Device) - Reedsville, PA (Onsite)Job Title - Manufacturing Quality Engineer (Medical Device) - Reedsville, PA (Onsite)

APN Software Services, IncCompany Name - APN Software Services, Inc

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Reedsville, Pennsylvania, USA

Contract

ONLY W2 Contract (No C2C) Position Title: Manufacturing Engineer Location: Reedsville Pennsylvania USA 17084 (Onsite) Duration:12 Months Hours per Week: 40 (8 hrs/day) Your Responsibilities In this role as a Manufacturing Engineer, you will focus primarily on releasing new products into manufacturing. In addition, you will play a key role in developing new manufacturing processes and implementing process controls. Your responsibilities will include, but are not limited to: Work collaboratively

R&D Engineer Sustaining, Medical Devices (Disposables) - Plymouth, MNJob Title - R&D Engineer Sustaining, Medical Devices (Disposables) - Plymouth, MN

Cube Hub, Inc.Company Name - Cube Hub, Inc.

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Plymouth, Minnesota, USA

Contract

Job Title: Principal R&D Engineer Sustaining, Medical Devices (Disposables) **Workers can be remote/hybrid but must be local and able to come into the office at least three days a week** Job Location: Plymouth, MN Job Duration: 12 months Summary: This section focuses on the main purpose of the job in one to four sentences. Technical lead for DHF structure within sustaining engineering for disposable medical devices. Essential Duties and Responsibilities: This section contains a list of prima

Medical Device Cleanroom TechnicianJob Title - Medical Device Cleanroom Technician

Vaco by HighspringCompany Name - Vaco by Highspring

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Full-time

Overview:This role involves handling, assembling, organizing, and documenting components used in medical devices for endoscopic procedures. The ideal candidate will demonstrate strong attention to detail, consistent reliability, and excellent fine motor skills. Working as part of a small team in an ISO 8 cleanroom environment, the technician will help ensure that quality and productivity targets are consistently achieved. Key Responsibilities: Accurately identify and organize the correct compone

Sales Engineer - Contract Medical Device - NHJob Title - Sales Engineer - Contract Medical Device - NH

Michael Page InternationalCompany Name - Michael Page International

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Somersworth, New Hampshire, USA

Full-time

Join a PE backed company with room for career advancementBe apart of a collaborative culture in the contract medical device space About Our Client Our client is a U.S.-based contract manufacturing and outsourcing company that provides comprehensive services to medical device, biotechnology, and pharmaceutical companies. Founded in 1997, it specializes in regulatory consulting, product sterilization, packaging, clean room assembly, and testing, helping clients accelerate time-to-market while en

Biocompatibility Manager - Medical Devices (on-site)Job Title - Biocompatibility Manager - Medical Devices (on-site)

Abbott LaboratoriesCompany Name - Abbott Laboratories

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Los Angeles, California, USA

Full-time

Senior Design Control, Software Quality Engineer (Medical Devices)Job Title - Senior Design Control, Software Quality Engineer (Medical Devices)

Abbott LaboratoriesCompany Name - Abbott Laboratories

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Alameda, California, USA

Full-time

W2 - Java (5+ years) with Automobile/Aero Space/Medical Device DomainJob Title - W2 - Java (5+ years) with Automobile/Aero Space/Medical Device Domain

KONNECTINGTREE INCCompany Name - KONNECTINGTREE INC

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Minneapolis, Minnesota, USA

Contract

W2 Role - No C2C Looking for 5+ years experience candidate apart from Internship / Partime roles (will not be calculated). Must have Experience: Automobile or AeroSpace or Medical Device Domain experience EAD share resume to

.Net Architect with Medical DevicesJob Title - .Net Architect with Medical Devices

DCM Infotech LimitedCompany Name - DCM Infotech Limited

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Merrimack, New Hampshire, USA

Contract

Architect: Architect and develop software systems for medical devices in compliance with IEC 62304. Design scalable solutions using C# .Net Core 8 and Service-Oriented Architecture (SOA) and microservices. Implement communication protocols with gRPC (Google Protocol Buffers) in SOA. Develop state machines for managing system workflows and behaviors. Optimize system performance and ensure design and architectural best practices. Create and maintain technical documentation, including architecture

Net Architect with Medical Devices - Onsite (Merrimack, NH)Job Title - Net Architect with Medical Devices - Onsite (Merrimack, NH)

MSYS Inc.Company Name - MSYS Inc.

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Merrimack, New Hampshire, USA

Contract

Title:Net Architect with Medical Devices - Onsite (Merrimack, NH) Location: Merrimack, NH, USA Length: Long term Restriction: W2 or C2C Description: Webcam interview; Long term project OnsiteLocal Or Nearer to NH Preferred Description: Architect and develop software systems for medical devices in compliance with IEC 62304.Design scalable solutions using C# .Net Core 8 and Service-Oriented Architecture (SOA) and microservices.Implement communication protocols with gRPC (Google Protocol Buff

Quality Assurance Engineer (Medical Device)Job Title - Quality Assurance Engineer (Medical Device)

Judge Group, Inc.Company Name - Judge Group, Inc.

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Framingham, Massachusetts, USA

Contract

Location: Framingham, MA Salary: $90,000.00 USD Annually - $105,000.00 USD Annually Description: Our client is currently seeking a Quality Assurance Engineer (Medical Device). This is a permanent, direct hire, on site role. Key Responsibilities: Investigate material nonconformance issues and resolve supplier concerns. Maintain calibration system and ensure compliance with 21 CFR 820 & ISO 13485. Support manufacturing engineering with documentation and process improvements. Assist in prod