R&D Engineer II
hace 4 semanas
About the Role:
We are seeking a highly skilled R&D Engineer II to support the design and development of products, materials, process changes, or new technology for projects with moderate to high complexity.
Your Responsibilities Include:
- Successfully completes complex engineering work in one or more of the following: product design and development, complex engineering tests and design experiments, preparation of specifications, product capability studies, research investigations, and process/test documentation through the product lifecycle.
- Develop solutions to a variety of problems of high complexity and scope where analysis of situations or data requires a review of identifiable factors.
- Summarizes, analyzes, and draws conclusions from test results. Designs and prepares complex reports to communicate results to the technical community.
- Translates customer needs into product requirements and design specifications.
- Responsible for engineering documentation.
- Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.
- May train, provide work direction, and supervise technicians and entry-level engineers.
- Works under general direction or within a team to complete projects and special assignments.
- Establishes and cultivates a range of business relationships to facilitate the completion of assignments. Influences project team and peers on business solutions.
- Cooperate in determining goals and objectives for projects. May lead projects within the function or department and/or represent the role in larger project teams.
- Performs troubleshooting on product problems related to design, material, or process.
Requirements:
- Bachelor's/Licenciature Degree: Mechatronics, Electronics, Electrical, Mechanical, Materials Science, Biomedical, Industrial, Chemical Engineering or related field.
- English level: +90%.
- Experience: +2 years in related positions.
- Knowledge of ISO 13485, MDR, and FDA medical device requirements, including design controls, product life cycle, validation/verification activities, and process improvement.
- Ability to travel internationally.
- Work Mode: Onsite.
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