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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

Software Architect

Motion Recruitment Partners, LLC

Boston, Massachusetts, USA

Full-time

Our client, a global leader in specialized diagnostics, is seeking an experienced Software Architect to drive the design and development of platform architecture across multiple product lines. This is a high-impact role focused on shaping scalable, reliable, and compliant software solutions within a regulated environment. Key Responsibilities: Lead the architecture and design of embedded and application-level software for medical device platforms.Ensure consistency in software architecture and d

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

Senior Algorithm Verification R&D Engineer

Boston Scientific Corporation

Maple Grove, Minnesota, USA

Full-time

Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your

Principal Systems Engineer

Abbott Laboratories

Pleasanton, California, 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 your family, be your true self, and live a full li

Principal Systems Engineer

Abbott Laboratories

Pleasanton, California, 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 your family, be your true self, and live a full li

System Validation 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 applicabi

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

Quality Assurance Engineer - Process and Validation

Civica Rx

Petersburg, Virginia, USA

Full-time

About Civica Civica is a 501(c)(4) social welfare organization established in 2018 by health systems and philanthropies to reduce chronic generic drug shortages and related high prices in the United States. Civica is led by an experienced team of healthcare and pharmaceutical industry leaders. Today, more than 55 health systems have joined Civica. They represent over 1,500 hospitals and one-third of all U.S. hospital beds. Civica has also begun to supply the U.S. Department of Veteran's Affairs

Senior Mechanical Engineer

Motion Recruitment Partners, LLC

Boston, Massachusetts, USA

Full-time

Our client, a leading medical device company, is seeking a Senior Mechanical Engineer to join their R&D team. This role involves contributing to the design, development, and support of diagnostic systems and electromechanical components in a regulated environment. The ideal candidate will have a strong background in mechanical design, experience with complex assemblies, and a track record of bringing products from concept through development and into manufacturing. This is a hands-on engineering

Validation Engineer/CSV Engineer

Katalyst Healthcares and Lifesciences

Walnut Creek, 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 applicabi

Engineer Disposables and Sustaining

Katalyst Healthcares and Lifesciences

Plymouth, Minnesota, USA

Full-time

Responsibilities: Create new 3rd party supplier documentation including design specifications, labelling, design drawings, etc. for peritoneal dialysis disposable sets. Create, modify, and maintain design history files. Perform change control assessments. Work closely with project manager and technical lead to achieve project commitments. Adhere to design control procedures, general safety rules, company policies and procedures, FDA and international regulations and guidance. Requirements:

Computer System Validation (CSV) Engineer

Katalyst Healthcares and Lifesciences

Remote or Massachusetts, USA

Full-time

Responsibilities: Lead and execute CSV activities across GxP-regulated systems (LIMS, MES, ERP, etc. Author and maintain validation deliverables: URS, FS, DS, IQ, OQ, PQ, and traceability matrices. Ensure systems comply with 21 CFR Part 11, EU Annex 11, and GAMP 5. Support system implementations, upgrades, and periodic reviews. Collaborate with QA, IT, and business users to drive validation strategy. Participate in audits and inspections to demonstrate compliance. Requirements: Bachelor's

Development Engineer

Katalyst Healthcares and Lifesciences

Cincinnati, Ohio, USA

Full-time

Job Description: Medical Devices | Component Development | Project Management Join a highly specialized team working on cutting-edge medical device development and manufacturing excellence. We're looking for a skilled Development Engineer with deep expertise in component qualification, cost reduction strategies, and plant transfer processes. Responsibilities: Drive design, development, and qualification of metallic and plastic medical device components. Lead project management and cross-functi

Sr Engineer, Embedded GUI Software

Masimo Corporation

Irvine, California, USA

Full-time

Job Description Job Summary: As an Embedded GUI Software Engineer, you will design, develop, and implement applications for our next generation patient monitoring devices. Day to day: Develop GUI applications for our medical devices Design, Implementation and Maintenance of Software Peer design/code review Software Documentation Software Specification and Testing Requirements: Strong fundamentals in computer graphics Experience with C++ software development experience Experience with graphica

Quality Engineer

Judge Group, Inc.

Deerfield Beach, Florida, USA

Contract

Location: Deerfield Beach, FL Salary: $85,000.00 USD Annually - $100,000.00 USD Annually Description: Job Title: Quality Engineer Location: Deerfield Beach, FL Our client is a global leader in self-injection device development, design, and manufacturing. With a team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to provide autoinjectors, pen injectors, and drug delivery systems. Headquartered in Switzerland since 2018, with operations in Sweden, Taiwan, an

Senior Compliance Software Engineer (Product)

Abbott Laboratories

Alameda, California, 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. Senior Compliance Software Engineer (Product) Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and fam

Sr. Quality Engineer

Judge Group, Inc.

Deerfield Beach, Florida, USA

Contract

Location: Deerfield Beach, FL Salary: $100,000.00 USD Annually - $120,000.00 USD Annually Description: Job Title: Senior Quality Engineer Our client is a global leader in self-injection device development, design, and manufacturing. With a team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to provide autoinjectors, pen injectors, and drug delivery systems. Headquartered in Switzerland since 2018, with operations in Sweden, Taiwan, and the US, we drive inn

Technical Writer

Cube Hub, Inc.

Batesville, Indiana, USA

Contract

Job Title Technical Writer Location - Batesville, IN Duration - 12 months with a possibility of extension Shift Details First Shift, Hybrid (In-office Tuesday, Wednesday, Thursday) Pay Range - $33/hr - $35/hr Job Description: Key Responsibilities Under supervision, edit, format, and proofread operational and instructional documents for medical devices Ensure documentation adheres to departmental style guidelines and quality standards Collaborate with Sustaining Engineering to upd

Product Quality Assurance Analyst III

Abbott Laboratories

Alameda, California, 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. Product Quality Analyst Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your tru