Medical devices Jobs

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Imaging Service Engineer 2

Sodexo

•

Highland Park, Illinois, USA

Full-time

Role Overview: Precise. Reliable. Powerful. Join a team as innovative as the technology we manage. Sodexo's Healthcare Technology Management (HTM) Division is looking for a highly skilled and confident individual to fulfill an Imaging Service Engineer II role located in Highland Park, IL. This person will inspect, repair, maintain, and calibrate basic diagnostic imaging equipment, devices, systems, and instruments. Interact on a routine basis with other clinical health providers in the identif
Posted 32 days ago | Updated 1 hour ago

Imaging Service Engineer 2

Sodexo

•

Highland Park, Illinois, USA

Full-time

Role Overview: Precise. Reliable. Powerful. Join a team as innovative as the technology we manage. Sodexo's Healthcare Technology Management (HTM) Division is looking for a highly skilled and confident individual to fulfill an Imaging Service Engineer II role located in Highland Park, IL. This person will inspect, repair, maintain, and calibrate basic diagnostic imaging equipment, devices, systems, and instruments. Interact on a routine basis with other clinical health providers in the identifi
Posted 32 days ago | Updated 7 hours ago

Quality Engineer

Advantage Technical

•

Arden Hills, Minnesota, USA

Full-time

Advantage Technical is hiring a Quality Engineer in Arden Hills, MN. Join a collaborative team focused on improving patient outcomes through data-driven investigations and continuous product improvement. Hours & Pay Pay Rate: $42.00/hour Schedule: 8:00 AM - 4:30 PM (42 hours/week) Work Model: Hybrid - 3 days onsite in Arden Hills In this role, you'll lead post-market investigations and signal escalations for Single Use Devices and Capital Equipment in the Peripheral Intervention/Vascular Surge
Posted 8 days ago | Updated 2 hours ago

Validation Engineer

Katalyst Healthcares and Lifesciences

•

Santa Clara, California, USA

Full-time

Roles & Responsibilities: Software quality assurance or software validation. Preferably within the medical device industry. Strong knowledge of FDA 21 CFR Part 820, ISO 13485, IEC 62304. Experience in non-product software validation. Includes tools for development, testing, maintenance. Deep understanding of quality standards and regulatory requirements: FDA 21 CFR Part 820. ISO 13485. IEC 62304. Software quality assurance. Software validation. Non-product software tools (for testing
Posted 13 days ago | Updated 5 hours ago

Engineer Sr. I - Extrusion - SC

Arthrex

•

Pendleton, South Carolina, 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
Posted 11 days ago | Updated 8 hours ago

Associate UX Content Strategist

Kforce Technology Staffing

•

Acton, Massachusetts, USA

Contract

RESPONSIBILITIES: Kforce has a client in Acton, MA that is seeking an Associate UX Content Strategist. Summary: We are seeking an Associate UX Content Strategist to join our UX team. This role is responsible for crafting engaging, informative UX content that enhances product experiences for a diverse audience-including patients, caregivers, and healthcare providers-helping simplify the lives of those impacted by chronic health conditions. As an Associate UX Content Strategist, you will elevate
Posted 4 days ago | Updated 4 hours ago

Software Engineer - Embedded C, C#, C++ | Marlborough, MA

Michael Page International

•

Marlborough, Massachusetts, USA

Full-time

Join a revolutionary medical device manufacturing organizationWork with a team making a difference to patients all over the world About Our Client The company is a medical device organization that design and develop cutting-edge software for complex medical devices. They have an FDA approved device that is live in the US, Europe & Asia and they're looking to further grow their R&D team with this hire, and plan to continue their growth for the remainder of 2025 and into 2026! Job Description
Posted 19 days ago | Updated 2 hours ago

SAP RAR (Revenue Accounting and Reporting) Consultant

Sage IT Inc

•

Franklin Township, New Jersey, USA

Contract, Third Party

Job Summary: We are seeking a highly skilled SAP RAR (Revenue Accounting and Reporting) Consultant with extensive experience in designing, configuring, and implementing SAP RAR solutions in compliance with IFRS 15 and ASC 606. This role requires deep expertise in RAR integrations with FI, and SD, modules, and a solid understanding of order-to-cash and revenue recognition processes in S/4 HANA environment. Key Responsibilities: Lead and support the implementation of SAP RAR including solut
Easy Apply
Posted 2 days ago | Updated 1 day ago

Mechanical Engineer

Katalyst Healthcares and Lifesciences

•

Batesville, Indiana, USA

Full-time

Job Description: As part of the sustaining engineering team, you will be responsible for design changes for medical device products such as hospital beds and equipment. The engineering design changes may be related to design improvements, new compliance requirements, or supply chain support. Responsibilities: As a mechanical engineer on the team, you will be responsible for performing design analysis and engineering releases for small to medium projects or participate in portions of larger comp
Posted 15 days ago | Updated 5 hours ago

Senior Post Market Engineer

Katalyst Healthcares and Lifesciences

•

Gainesville, Florida, USA

Full-time

Roles & Responsibilities: Bachelor's Degree in an Engineering discipline from an accredited institution required. Complaint product analysis and testing per procedures and requirements. Root cause analysis and supports conclusions with objective evidence and sound rationale. Complaint risk analysis and complaint history reviews. Knows and applies Quality System requirements and any appropriate FDA and international standards. Must have an understanding of root cause and risk analysis as wel
Posted 60+ days ago | Updated 5 hours ago

Quality Specialist II

Sunrise Systems, Inc.

•

Lititz, Pennsylvania, USA

Contract

Job Title: Quality Specialist II Job ID: 25-08786 Location: Lititz, PA 17543 Duration: 16 Months On W2 Contract Description: The Quality Specialist II will be accountable to support Product Review reports and to support investigations pertaining to observations or trends discovered during data collection. The Quality Specialist II will also be accountable for supporting Laboratory Information Management System (LIMS) Master Data changes needed by the Quality Control Laboratory. Key Responsibilit
Easy Apply
Posted 47 days ago | Updated 1 day ago

Validation Engineer

Katalyst Healthcares and Lifesciences

•

Libertyville, Illinois, USA

Full-time

Responsibilities: Lead validation efforts for injection molding machines, auxiliary equipment (e.g., dryers, chillers, robots), and integrated automation systems. Develop and execute validation protocols (SAT, FAT, IQ, OQ, PQ) for molding and downstream equipment. Support the qualification of new production lines involving injection-molded components. Perform process characterization, capability studies, and stability testing for moulded parts. Collaborate with tooling, manufacturing, and q
Posted 14 days ago | Updated 5 hours ago

Engineer II, Quality & Organizational Excellence

Thermo Fisher Scientific

•

Los Angeles, California, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The Engineer II, Quality is responsible for creating a 1st class quality culture by enabling peer ownership of CAPAs, Quality Plans, Training, and PPI events. This position will drive these items with process owners to ensure timely and effective completion of required activities. Additionally, this role with assist in driving quality excellence through execution of Quality Evolution initiatives, own meaningful q
Posted 17 hours ago | Updated 5 hours ago

Principal Engineer

Katalyst Healthcares and Lifesciences

•

Plymouth, Minnesota, USA

Full-time

Job Description: 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. Responsibilities: This section contains a list of primary responsibilities of this role that account for 5% or more of the work. The incumbent will perform other duties assigned. Manage a new 3rd-party supplier documentation strategy for peritoneal dialysis disposable sets. Manage change controls from init
Posted 23 days ago | Updated 5 hours ago

Technical Writer - Pittsburgh, PA - $70k per annum - fulltime

MetaSense, Inc.

•

Pittsburgh, Pennsylvania, USA

Full-time

PRINCIPAL RESPONSIBILITIES: 2+ years of experience as a Technical Writer (for SOP, QMS etc.) in the medical device industryPractical knowledge of standards and regulations pertaining to the medical device industry.Experience with CAD and VisioYou will be trained on client products and SOPs / templatesMaintain a backlog of all change requests to client's QMS design controls procedures/WIs/forms, in response to CAPAs or for efficiency improvements.Plan and execute the defining the specific procedu
Easy Apply
Posted 51 days ago | Updated 25 days ago

Warehouse Associate II - International Fulfillment

Arthrex

•

Fort Myers, Florida, 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
Posted 9 days ago | Updated 8 hours ago

Quality Technician

Advantage Technical

•

Arden Hills, Minnesota, USA

Full-time

Join the Team as a Quality Technician! Step into an impactful role where your attention to detail and technical skills can make a difference. Advantage Technical is hiring a Quality Technician in the Roseville, MN, area to support post-market complaint investigations for medical devices. If you are ready to be hands-on, work collaboratively, and ensure the highest standards of quality, this opportunity is for you! Pay & Schedule: Pay Rate: $27.00 per hour Hours: Monday - Friday, 8:00 AM - 4:30
Posted 4 days ago | Updated 2 hours ago

Principal Custom Test Systems Engineer- ME (ONSITE)

Stryker

•

Portage, Michigan, USA

Full-time

Work Flexibility: Onsite As a Principal Test Systems Engineer you will act as a primary point of contact for the design, development, fabrication, and implementation of electro-mechanical test systems to aid in the development and verification testing of new medical devices. You will be responsible for establishing system level strategies for the development of new custom test equipment, coordinating closely across functional areas to ensure alignment, helping to set direction and engineering s
Posted 5 days ago | Updated 5 hours ago

Sterility Engineer

Philips North America

•

Plymouth, Minnesota, USA

Full-time

Job Title Sterility Engineer Job Description The Sterility Engineer is responsible for supporting the ethylene oxide sterilization program, critical to current NPI/Sustaining initiatives for Philips' Image Guided Therapy Devices (IGTD) business. Your role: Assists with managing the ethylene oxide sterilization program that includes new validations, supporting ongoing production sterilization activities and annual requalification's.Conducts in-depth reviews of technical documentation, includin
Posted 21 days ago | Updated 6 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Omaha, Nebraska, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 22 days ago | Updated 5 hours ago