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Medical Device Manufacturing Engineer Jobs in California

Sr. Medical Device Manufacturing Design Engineer (Min 5+ Years Exp/Must Have Exp In Catheters, Implants, Ancillary Products Or Similar)- Greencard Or Usc
By JobsPro Staffing (JPS) At Campbell, CA, United States
Required Skills, Abilities & Experience
Design, execute, and analyze experiments using sound statistical methodology. Participate in risk management activities, including development and ownership of process FMEAs.
Experience with quality system documentation requirements and test protocols.
Develop manufacturing processes by applying engineering knowledge and product design, fabrication, assembly, tooling, and materials.
Improve manufacturing efficiency through planning and evaluation of workflow, space requirements and equipment layout.
Calculate production, labor, and material costs; manage and adjust production schedules to meet demand.
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 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).
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.
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 Manufacturer
By Jobot At Anaheim, CA, United States
Collection and trending of key quality indicators for management review.
ASQ Certifications such as Manager of Quality/Organizational Excellence, Quality Engineer, Quality Auditor, Supplier Quality Professional, etc.
Conduct internal quality audits to ensure compliance to Quality System and regulatory requirements.
Facilitate receiving inspection and first article inspection activities. Help establish receiving inspection requirements for materials and any needed
Facilitate calibration activities. Help establish calibration requirements for measuring equipment and test fixtures as needed.
Assure Quality System Processes are in compliance with US-FDA, MDD/MDR, ISO 13485 and other applicable country specific medical device
Validation Quality Engineer Ii (Medical Device)
By STAAR Surgical At Monrovia, CA, United States
• Excellent project management, organization, writing, communication and presentation skills required.
10. Compile Quality metrics, analyze trends and report to Quality Management.
13. Perform additional duties as assigned by Management.
• Bachelor’s degree, preferably in Engineering or sciences or equivalent combination of education/experience.
9. Coordinate contractor qualification activities with appropriate departments.
• Experience in vision care or intraocular lens industry preferred.
Validation Quality Engineer (Medical Device)
By STAAR Surgical At Lake Forest, CA, United States
•Excellent project management, organization, writing and presentation skills required.
.Prepare and report appropriate metrics to executive management.
•Demonstrated expert knowledge of Windows-based software, including Word, Excel, Access, Project, and Power Point.
•A Bachelor of Science (BS) in science or engineering, advanced degree preferred.
•Solid understanding of investigation techniques including design of experiments and root cause analysis.
•Demonstrated understanding and application of Quality System Auditing and Analysis
Medical Device Engineer Jobs
By LINQM, Inc. At Irvine, CA, United States

LINQM is looking for a Medical Device Engineer. Write, Develop, execute experiments and tests, create, validate, and improve product designs and Ownership in the process validation in (IQ - ...