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Verification Engineer (Embedded Medical Device)

Katalyst Healthcares and Lifesciences

Burlington, Massachusetts, USA

Full-time

Job Description: Drive verification and validation in software/hardware testing for medical device products. This role is critical to ensuring the quality and reliability of products by leading test strategy, planning, execution, and automation efforts. The Test Lead will collaborate closely with development teams, product leadership, and other stakeholders to establish best practices, enhance testing efficiency, and improve overall product performance. Responsibilities: Define and implement

Senior Automation Engineer - Medical Devices (IL or TX)

Flextronics

Buffalo Grove, Illinois, USA

Full-time

Job Posting Start Date 07-15-2025 Job Posting End Date Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary. Job

Sr. R&D Sustaining Engineer (medical device)

Katalyst Healthcares and Lifesciences

Austin, Texas, USA

Full-time

Responsibilities: Designs and engineers the solution down to detail to satisfy the specified requirements of the customer. Defines the products, components and systems to be used and their concrete characteristics. Configures the components and systems of the solution according to the requirements. Develops detailed solutions for the integration to ensure the interaction of the individual elements as a functioning unit. Is responsible for the realization of the solution with the required functio

Mechanical Engineer II-Medical Device Solutions

Battelle Memorial Institute

Columbus, Ohio, USA

Full-time

Battelle delivers when others can't. We conduct research and development, manage national laboratories, design and manufacture products and deliver critical services for our clients-whether they are a multi-national corporation, a small start-up or a government agency. We recognize and appreciate the value and contributions of individuals from a wide range of backgrounds and experiences and welcome all qualified individuals to apply. Job Summary We are currently seeking a Mechanical Engineer I

Medical Device & Regulations Engineer

Katalyst Healthcares and Lifesciences

Santa Clara, California, USA

Full-time

Responsibilities: Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development. Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software. Support audits and inspections by regulatory bodies, ensuring that non-product software systems comply with quality and documentation standards. Ensure computerized systems are appropriately validated Assessment of applicabil

Senior/Staff Digital Electrical Engineer - FPGA for Medical Devices (San Diego, CA)

Philips North America

San Diego, California, USA

Full-time

Job Title Senior/Staff Digital Electrical Engineer - FPGA for Medical Devices (San Diego, CA) Job Description Senior/Staff Digital Electrical Engineer - FPGA for Medical Devices (San Diego, CA) As a member of an international cross-functional team, you work closely together with electrical engineers, transducer engineers, system engineers, and ultrasound engineers on the development of Intravascular Ultrasound Systems. Your role: Conceptualizing, designing, and developing FPGAs and digital

R&D Engineer with Medical Device

Katalyst Healthcares and Lifesciences

Irvine, California, USA

Full-time

Job Description: We are seeking a motivated and innovative R&D Engineer to support the design, development, and testing of medical devices in compliance with FDA and ISO standards. The ideal candidate will work closely with cross-functional teams to bring new products from concept to commercialization. Responsibilities: Design and develop medical devices and components from concept to production. Create design inputs, outputs, risk analysis, and test protocols. Perform design verification and

R&D Application Software Engineer - C++ & Python for Medical Device (Cambridge, MA)

Philips North America

Cambridge, Massachusetts, USA

Full-time

Job Title R&D Application Software Engineer - C++ & Python for Medical Device (Cambridge, MA) Job Description R&D Application Software Engineer - C++ & Python for Medical Device (Cambridge, MA) Join the Breakthrough Innovation Teams (BRITE) at Philips to build next-gen surgical robots and bring better care for more people. BRITE is the embodiment of Philips' approach to driving breakthrough innovation by accelerating innovation to nurture nascent projects from early innovation stage to full a

Mechanical Engineer with Medical Device

Katalyst Healthcares and Lifesciences

Irvine, California, USA

Full-time

Roles & Responsibilities: Mechanical Engineering Degree. Quality Control exposure. ISO 13485 awareness (not mandatory). College Graduate (s) to (less than) 10 years of experience. Experience with relevant Supplier Quality requirements is added advantage. Management of supplier Quality lifecycle Support. Engineering documents Pre-review Support. Supplier NC/CAPA lifecycle Management Support. Quality Agreement update Support. Weekly/Monthly Project progress dashboard generations. Procedures/SOPs u

Sr. Engineer Disposables R&D, Sustaining (Hybrid)

DivIHN Integration Inc.

Plymouth, Minnesota, USA

Contract

DivIHN (pronounced divine ) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent. Visit us at to learn more and view our open positions. Please apply o

Principal Software Engineer

Jobot

Rockville, Maryland, USA

Full-time

A rapidly growing 800 Person Medical Device company is currently hiring for a fully remote Principal Software Engineer with full-stack Java experience! This Jobot Job is hosted by: Ryan Sullivan Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $150,000 - $180,000,000 per year A bit about us: A rapidly growing 800 Person Medical Device company is currently hiring for a fully remote Principal Software Engineer with full-stack Java experience!

Senior Python Developer

Jobot

Rockville, Maryland, USA

Full-time

A rapidly growing 1000 person Bio-tech company is hiring multiple Python/Java Developers with experience developing applications for Medical Device, Instruments, or other stand alone Devices! This Jobot Job is hosted by: Ryan Sullivan Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $150,000 - $175,000 per year A bit about us: A rapidly growing 1000 person Bio-tech company in Rockville, MD is hiring multiple Python/Java Developers with exper

Senior Principal Engineer.

Pyramid Consulting, Inc.

Round Lake, Illinois, USA

Contract

Immediate need for a talented Senior Principal Engineer. This is a 12+ months contract opportunity with long-term potential and is located in Round Lake, IL(Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-79882 Pay Range: $74 - $75/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Leads cross functional

IQ/OQ/PQ Validation Engineer with Medical (W2)

Sovereign Technologies

Irvine, California, USA

Full-time

Title: Sr. Validation engineer with Medical Device Candidates Location: Onsite in Irvine, CA Duration: 2+ years 1) Word copy of resume 2) 2-3 professional references THIS IS NOT A SOFTWARE POSITION Looking for hands on IQ/OQ/PQ Validation in Medical Device Candidates MUST HAVE Bachelor of Science in Engineering or a related subject with 4+ years of experience in validation GMPs.Good understanding of engineering and machine tool fundamentals.Written and owned the validation processSME on IQ/OQ/PQ

Principal Engineer

Aditi Consulting

New Albany, Ohio, USA

Contract

Payrate: $45.00 - $49.00/hr. Summary: Lead teams in the development of drug delivery devices. Scope includes a wide range of devices, such as; needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems. The qualified candidate will lead technical teams to ensure successful device development of these mechanical and electro-mechanical medical devices. The Principle Engineer will work closely with team members to develop detai

Computer System Validation

Smart Source Technologies

Jacksonville, Florida, USA

Contract

Computer System Validation Jacksonville, FL Onsite 12 months contract Pay : $55/hr W2 or $60/hr C2C Job Description:- Working knowledge of FDA and European medical device regulations (QSR and ISO) is required. Working knowledge of software validation requirements for software used in the production of medical devices and software used to support the Quality System is required. Working knowledge of GAMP5 and SDLC is required. Working knowledge of regulations for electronic records, electronic

Systems Engineer

Bytecubit Technologies

White Bear Lake, Minnesota, USA

Contract

Job Title: Systems Engineer Location: White Bear Lake, MN Duration: 6 months + extension Pay rate: $45/hr -$70/hr (depending on experience) Job Description: Looking for a Systems Engineer/ Technical Lead with medical device experience (preferably Class II, ) Client Facing experience Systems Engineer experience around Risk Management, Systems Architecture, ongoing verification, layout work in CAD packages. Software - MATLAB, Python scripting and MINITAB Candidate must have direct electrical desi

Senior Regulatory Affairs Specialist

Sunrise Systems, Inc.

Chaska, Minnesota, USA

Contract

Our client, a leading medical devices manufacturing company, is looking for a Senior Regulatory Affairs Specialist. This is for an initial duration of 18 months and is located in Chaska, MN. Job Type: Contract (Candidates must be able to work on W2 without VISA sponsorship) 3 must haves: Experience with design changes, demonstrated RA leadership on high visibility core team, IVDR or EMDR experience Job Description: The Senior Specialist Regulatory Affairs is an individual contributor and subject

(2) Process Engineer - SAP Implementation

Primary Talent Partners

Dexter, Michigan, USA

Contract

Primary Talent Partners has an exciting opportunity for TWO SAP Engineers in Dexter, MI to help assist our Medical Device client with a major SAP implementation. Please see details below and apply if qualified and interested!Logistics:Client: Confidential Medical Device ManufacturerJob Title: SAP Implementation Engineer - Documentation & BOMsLength: 6-month contract (possible extension)Location: Dexter, MI - 100% onsiteSchedule/Hours: Full-time, standard business hoursPay Range: $55-$70/hr on ou

.Net Architect

PeopleNTech

Merrimack, New Hampshire, USA

Third Party, 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