Register
Recruit Create CV

Medical Device Engineer Jobs

Qa Engineer - Med Device
By Hays At Acton, MA, United States
• Perform quality duties as assigned by Quality Manager III.
• 0-3 years of Medical Device experience
• Knowledge and working application of reading and understanding blueprints and technical drawings.
• Ability to multi-task and methodically manage projects.
QA Engineer - Med Device – Contract – Acton, MA - $39.00-$49.00/hr.
• Complaint Investigations (Time Spent: 45%):
Medical Device Tester Jobs
By Peritus Inc At St Paul, MN, United States

Experience in verification/testing is preferred.

medical device domain or related industry

R&D Medical Device Engineer
By Abras Life sciences At Dallas, TX, United States
2-3 years of relevant experience in Research and Development within the Medical Device Industry.
Independently conduct smaller approved projects, making suggestions for improvements based on current technical knowledge.
Strong multitasking skills to work efficiently under pressure and meet project deadlines.
Bachelor's Degree in Engineering or a related field from an accredited university.
Solve routine design and engineering challenges with minimal assistance, demonstrating technical expertise in your field.
appropriate techniques and methods to complete assignments within negotiated deadlines, following general instructions.
Technical Support Specialist - Medical Device
By R92 At United States
1 -2 year experience in medical device industry background
Proactive and results-oriented who can work independently and as part of a team to effectively manage assignments and support customer queues.
Must have excellent verbal and written communication skills.
Good interpersonal skills with the ability to react quickly, accurately, and remain calm under pressure.
1- 2 years related experience providing technical support
Experience using mobile devices such as cell phone, laptop and tablet to perform work activities
Medical Device Verification Engineer (Not A Qa Role)
By Systems Ally At San Jose, CA, United States
1) Python (hands on, able to build automation)
Design and Implement appropriate test protocols, test harnesses and test automation tools
Work with complex electro-mechanical systems, deploying new software releases and running the test protocols on the systems
Write thorough test plans/test protocols, test cases, test scripts and test scenarios.
Submit FDA valid documents and reports for all the products mentioned above.
Have a good understanding of FDA forms and protocols is a plus
Quality Management System - Medical Device
By Tesla BioHealing At Milford, DE, United States
Professional certifications related to quality management (e.g., ASQ Certified Quality Auditor, Certified Quality Manager) are a plus.
Proven experience in quality management, quality assurance, or regulatory compliance roles.
Design, implement, and maintain the Quality Management System to comply with relevant industry standards, regulations, and best practices.
Generate regular reports and metrics to communicate the effectiveness of the QMS to management.
Bachelor's degree in a relevant field (Quality Management, Engineering, Life Sciences, etc.).
Strong understanding of quality management principles, methodologies, and best practices.
Medical Device Quality Systems Coordinator
By Akkodis At Mount Prospect, IL, United States
Medical Device Quality Systems Coordinator job responsibilities include:
• Three plus years experience in the Medical Device Industry.
• Solid experience working in a Class I and Class II Medical Device environment.
• Extensive knowledge of medical device regulations/standards including 21 CFR 820 (QSR) and ISO - 13485:2016.
Pay/Salary Range: $40.00 and $45.00 per hour.
• MasterControl Maintenance - New employee set-up, Employee terminations, Password resets, Administrative back-up.
Device Test Engineer Jobs
By TechFetch.com - On Demand Tech Workforce hiring platform At Richardson, TX, United States

"ALL our jobs are US based and candidates must be in the US with valid US Work Authorization. Please apply on our website directly." Job Title: Device Test EngineerLocation: Atlanta, GA (Onsite) Job ...

Quality Engineer Ii - Medical Device
By Abbott Laboratories At , Santa Clara $72,100 - $144,100 a year
Ensures compliance to site level policies and procedures by promptly reporting non-compliance issues to management within Division and Corporation as appropriate.
Maintains vigilance to ensure adherence to Quality Policy and Quality system procedures by promptly reporting noncompliance issues to management.
Risk Management - Applies basic Risk Management principles to work.
Participates in the development or modification of Risk management files.
Complaint Evaluation - Investigates complex complaints with management oversight.
Participates in the development or modification of validation packages, design plans, and risk management deliverables (e.g.FMEAs).
Medical Device Assembler Jobs
By Diversatek At , Highlands Ranch, 80129 $22 - $27 an hour
Gather, maintain, and compile shop orders and technical data from production tests as necessary to fulfill documentation requirements.
At least 5 years of experience as an assembler working in research and/or production environment
Strong verbal and written communications skills
Must be a highly detail-oriented person with strong organizational and strong communication skills.
Building and testing electromechanical assemblies in a production environment following good manufacturing practices.
Become an expert in all areas of the production process with the ability and flexibility to perform in each process area
Medical Device Tester Jobs
By Abbott At Irving, TX, United States
Some laboratory or diagnostics experience desired.
Ability to demonstrate competency of computer skills.
B.S. in Computer Science or similar engineering discipline including Software Engineering, Biomedical Engineering, or Laboratory Science desired.
Title- Medical Device Tester I
Timings- 8am to 5 pm
Device Engineer Ii Jobs
By Pfizer At , Parsippany
Proactive, has experience with high performance teams, strong interpersonal and project management skills
Knowledge and experience with Drug Product processing and equipment
Perform other tasks necessary to support site compliance to Center and regulatory requirements.
Working knowledge of Food and Drug Administration Regulations, and Good Manufacturing Practices
Strong written and verbal communication skills
Demonstrated experience in a relevant manufacturing environment
Staff Engineer, Hardware, Mechanical R&D - Medical Device
By Werfen At , San Diego, 92121
Solidworks Data Management experience is required.
Minimum Knowledge & Experience required for the position:
Eight (8) years previous relevant industry experience required, preferably within a regulated medical device or pharmaceutical environment.
Evaluate and select appropriate components and technologies, considering both performance and manufacturing requirements.
Experience with the following tools/methods: FEA, Six Sigma, DOE, FMEA, Minitab, Arduino, Word, Power Point, Excel is highly desired.
Provide technical leadership to project teams.
Medical Device Defense Engineer
By HonorHealth At , Scottsdale, 85258

Overview: Looking to be part of something more meaningful? At HonorHealth, you’ll be part of a team, creating a multi-dimensional care experience for our patients. You’ll have opportunities to make ...

Quality Engineer(Medical Device, Otc, Drug + Cosmetic) - Hartland, Wi
By Medline Industries Inc At , Hartland
Experience using time management skills to prioritize, organize, and track details in order to meet deadlines of multiple projects.
Knowledge / Skills / Abilities
Provide Quality expertise in Product Development, Design Control activities, Risk Management, and CE Technical Files.
At least 2 years of experience in the Quality or Engineering.
Experience problem solving, overcoming obstacles, and reaching a positive and successful solution through mathematical or systematic operations.
Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook ).
Chemical Engineer Medical Device
By BD At , Glens Falls
Knowledgeable on materials for product designs in areas of responsibility.
Demonstrates strong communication skills across all levels of the organization, both internal and external.
General knowledge of basic physics and chemistry.
Basic knowledge of structure-property-process relationships of polymer systems.
Hands on experience working in a polymer chemistry laboratory.
Experience in a regulated environment.
Director Of Quality - Medical Device
By EPM Scientific At United States
A minimum of 8 years of experience in quality management within the medical device industry, including leadership roles.
Lead a team of quality professionals, including hiring, training, and performance management, to create a culture of excellence and collaboration.
Certified Quality Manager (CQM), Certified Quality Engineer (CQE), or other relevant certifications are a plus.
Lead and manage internal and external quality audits, ensuring compliance with regulatory standards and driving corrective and preventive actions as needed.
Proven track record of leading successful quality teams and managing complex projects in a remote or virtual work environment.
Excellent communication skills, with the ability to collaborate effectively with cross-functional teams and communicate complex quality concepts to diverse audiences.
Sr Medical Device Engineer
By Dexcom At , San Diego, Ca $91,400 - $152,300 a year
You have knowledge and direct experience handling raw and processed datasets of various sizes
You bring a track record of demonstrated knowledge and experience in biosensor development and testing
You have experience with modeling stochastic processes (Monte Carlo or similar)
You have strong analytical and experimental skills for characterization of materials and biosensor components
You have excellent collaboration, communication (written and verbal), and interpersonal skills
A full and comprehensive benefits program.
Quality Engineer (Medical Device)
By Regeneron At , East Greenbush, Ny
You have experience with device risk management activities
Participating in device risk management activities including UFMEA, DFMEA, PFMEA
You have knowledge of the combination device development process
Reviewing design and development paperwork and records for compliance to internal procedures and regulations
Ensuring accurate justification of statistical analysis and hypothesis testing
Reviewing technical reports as well as documents for Design History Files
Equipment Validation Engineer(Medical Device)
By Saraca Solutions At , , Nj
Must have experience in medical device process and equipment validation
Experience in medical device technical writing
Experience is ISO 13485, ISO 14971, 21 CFR Part 11
Follow all safety and current Good Manufacturing (cGMP) requirements within the plant
Develop and execute Field Acceptance Testing (FAT) and Site Acceptance Testing (SAT) using User Requirement Specifications (URS)
Lead validation engineering activities including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities

Are you looking for an exciting opportunity to use your engineering skills to make a difference in the medical field? We are looking for a Medical Device Engineer to join our team and help us develop innovative medical devices that improve patient care. If you have a passion for engineering and a desire to make a positive impact on the lives of others, this could be the perfect job for you!

Overview Medical Device Engineers are responsible for designing, developing, and testing medical devices and equipment. They must ensure that the devices meet safety and performance standards, as well as regulatory requirements. They must also be able to troubleshoot and repair any issues that arise with the devices. Detailed Job Description Medical Device Engineers are responsible for designing, developing, and testing medical devices and equipment. This includes researching and analyzing customer needs and requirements, developing prototypes, and conducting tests to ensure that the device meets safety and performance standards. They must also be able to troubleshoot and repair any issues that arise with the devices. In addition, they must be able to create and maintain documentation for the device, such as user manuals and technical specifications. Job Skills Required
• Knowledge of medical device design and development
• Knowledge of medical device regulations and standards
• Knowledge of medical device testing and troubleshooting
• Ability to use CAD software
• Ability to use statistical analysis software
• Ability to work independently and as part of a team
• Excellent problem-solving skills
• Excellent communication and interpersonal skills
Job Qualifications
• Bachelor’s degree in engineering, biomedical engineering, or a related field
• Experience in medical device design and development
• Knowledge of medical device regulations and standards
• Knowledge of medical device testing and troubleshooting
• Ability to use CAD software
• Ability to use statistical analysis software
Job Knowledge
• Knowledge of medical device design and development
• Knowledge of medical device regulations and standards
• Knowledge of medical device testing and troubleshooting
• Knowledge of medical device safety and performance standards
• Knowledge of medical device documentation
Job Experience
• Experience in medical device design and development
• Experience in medical device testing and troubleshooting
• Experience in medical device documentation
Job Responsibilities
• Design, develop, and test medical devices and equipment
• Research and analyze customer needs and requirements
• Develop prototypes and conduct tests to ensure that the device meets safety and performance standards
• Troubleshoot and repair any issues that arise with the devices
• Create and maintain documentation for the device, such as user manuals and technical specifications
• Ensure that the device meets regulatory requirements