Overview
On Site
$50 - $70
Contract - Independent
Contract - W2
Contract - 12 Month(s)
Skills
Clinical Trials
Electrical Engineering
Medical Devices
Manufacturing
Quality Assurance
Project Management
Risk Management
Research and Development
Verification And Validation
Job Details
Job Title - Principle Quality Engineer
Job Location - , Irvine, California,
Job Description -
Nice to Have:
- Experience with exploratory, early stage in-human clinical trials.
- Self-motivated, driven and committed to a team approach
- Strong interpersonal, organizational and project management skills
- Strong oral, presentation and technical writing skills.
- Ability to dissect, condense, and disseminate information appropriately to key stakeholders.
Main Key Skills:
- Experience with Risk Management for medical devices.
- Experience with electrophysiology/electrical/electromechanical medical device.
- Experience with Regulations for electromechanical medical devices.
Responsibilities may include the following and other duties may be assigned.
- Collaborates with cross OU to harmonize the design quality requirements/deliverables/procedures and implement to the program.
- Experienced in the areas of electrophysiology/electrical/electromechanical engineering design medical device / regulation
- Develops, modifies, applies and maintains quality standards and protocol for verification and validation during design/development process.
- Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
- Advices and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
- Create and maintain the risk register on a developing product and communicate to the stakeholders.
- Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
- Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
- May specialize in the areas of electrophysiology, electrical engineering design, incoming material, protocols, performance evaluation and reliability, research and development as they apply to product or process quality.
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