- 1 year of professional experience in the medical device field.
- Design Verification experience, specifically releasing and writing DV plans/reports for medical devices.
- Bachelor's degree in engineering required (Biomedical Engineering strongly preferred).
- 1 plus years of relevant work experience with a bachelor's degree, master's preferred
- 1-3 years of experience required.
- Prior experience as an engineer in a medically regulated industry
- Design verification and validation experience in the medical device industry
- Basic understanding of SolidWorks CAD system
- Exposure to failure mode analysis.
- PPK, MLTL, or any base-level knowledge of statistical tools or analysis.
- Test method validation
- Design verification (plans & protocols), reporting, and testing
- Data failure analysis on the design verification testing
- Work with accelerated and real-time aging
- Good computer skills in usage of MS Office Suite; CAD experience preferred.
- Good documentation, communication (e.g., written and verbal), and interpersonal relationship skills including consultative and relationship management skills.
- Basic understanding of statistical techniques
- Previous experience working with lab/industrial equipment required (if applicable)
- Solid understanding and knowledge of principles, theories, and concepts relevant to Engineering
- Solid problem-solving, organizational, analytical, and critical thinking skills
- Solid understanding of processes and equipment used in assigned work.
- Knowledge of and adherence to the client's Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing.
- Strict attention to detail
- Ability to interact professionally with all organizational levels.
- Ability to manage competing priorities in a fast-paced environment.
- Must be able to work in a team environment, including the ability to manage vendors and project stakeholders.
- Ability to build productive internal/external working relationships.
- Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of the environment and prevent pollution under their span of influence/control.
- Test, and/or improve products by developing moderately complex experiments and tests (including writing and executing protocols), analyze results, make recommendations, and develop reports, based on engineering principles - 25%
- Generate work instructions, test methods, engineering drawings/prototypes, etc. to establish/ characterize product and/or process specifications -25%
- Create/update portions of design control documents including requirement specs and risk documents - 20%
- Assign R&D support tasks; gives instruction to technicians on conducting tests; train technicians and provide feedback; and coordinate technician work - 15%
- Identify, evaluate, manage, and provide guidance to suppliers, including establishing tolerances and defining acceptance criteria for suppliers - 10%
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R&D Engineer I - Santa Ana, United States - TalentBurst
Description
Position: R&D Engineer I,Req#: 6477-1Location: Irvine, CA (100% onsite)
Duration: 12 Months Contract
Top Skills:
Applies knowledge of technical principles and the client's systems/procedures to maintain and optimize CC legacy products.
Education and Experience:
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