Design Quality Engineer
$105k - $135kTAE Life Sciences
Do Epic Science TAE is the world’s first private fusion energy company, founded in 1998 to commercialize the cleanest, safest, most affordable, and sustainable form of carbon-free power. We are applying science and engineering to design transformational technologies. Whether it's harnessing fusion through the science of stars, making exponential leaps in power efficiency, or innovating medical care with a novel cancer treatment: We're turning the promise of science into reality. We’re looking for candidates who are passionate about realizing our mission: A future where all people have affordable access to reliable, abundant, and environmentally friendly fusion-generated electricity. About The Role
Our podcast Good Clean Energy
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LinkedIn TAE Technologies is an Equal Opportunity Employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. We ensure all individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us View email address on click.appcast.io to request accommodations or request more information. Note to Agencies: TAE prefers to hire directly and maintains an existing preferred supplier list. We do not accept speculative CVs or referrals from agencies. If speculative CVs are sent, no fee will be applicable. Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
- Trains to all Quality System documents assigned in the applicable training plan.
- Authors, Updates, and Maintains all Quality Management System documents concerning Design Controls.
- Represents the Quality function as needed in meetings concerning design controls.
- Maintains a working knowledge of all applicable international standards concerning design controls.
- Develops plans for verification, validation, and useability activities in accordance with standards and directives.
- Reviews all product-level, system and sub-system-level, and component-level requirements for completeness and testability.
- Creates test cases to validate product-level requirements and to verify system-level requirements. Also capable of creating test cases for lower level requirements when necessary.
- Creates protocols for assessing useability of applicable requirements.
- Maintains traceability of subject requirements to the test cases that verify or validate them.
- Executes test cases on appropriate systems and accurately records the results.
- Enters defects into a defect tracking system when a system deficiency is encountered, providing sufficient detail for a development engineer to recreate and address the defect.
- Prepares appropriate reports to summarize the results of all testing activities.
- Other duties assigned by leadership
- Bachelor's degree (BS) in technical or life science field.
- Minimum of 5-7 years of experience in a medical device quality system (i.e., ISO 13485, 21 CFR Part 820).
- Excellent writing skills including authoring and editing operating procedures, work instructions, test plans, test cases/protocols, and test reports.
- Strong analytical and problem-solving skills, demonstrating sound judgment and understanding of strategic context with excellent attention to detail.
- Experience interacting and supporting cross-functional teams to achieve successful outcomes.
- Expertise in MS Office Suite.
- Results-oriented, positive “can-do” attitude with demonstration of appropriate urgency and initiative.
- Experience in complex computer-controlled, electro-mechanical medical devices is preferred.
- Radiation oncology device experience is preferred but not required.
- Capable of working onsite at our Orange County (Irvine) location.
- Ability to travel overseas to customer installations. Current passport desired.
- Ability and desire to travel for testing activities up to 90 calendar days per year.
- Capable of working in safe proximity to residual radiation (with proper PPE).
- Capable of climbing steps (less than 30) around medical device.
Our podcast Good Clean Energy
LinkedIn TAE Technologies is an Equal Opportunity Employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. We ensure all individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us View email address on click.appcast.io to request accommodations or request more information. Note to Agencies: TAE prefers to hire directly and maintains an existing preferred supplier list. We do not accept speculative CVs or referrals from agencies. If speculative CVs are sent, no fee will be applicable. Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
Vacancy posted 4 days ago
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