R&D Medical Device Engineer

As an R&D Medical Device Engineer, they will play a vital role in our organization's research and development efforts within the Medical Device Industry. Your primary responsibilities will include performing routine engineering assignments, documenting development work, and contributing to the planning and execution of projects. You will be expected to work independently on smaller approved projects while collaborating with cross-functional teams and adhering to regulatory standards.

Responsibilities

1. Execute routine engineering tasks that are part of larger projects, ensuring they are completed on time and within scope.
2. Prepare detailed documentation, including specifications for manufacturing and scientific test results, to maintain a comprehensive record of development work.
3. Solve routine design and engineering challenges with minimal assistance, demonstrating technical expertise in your field.
4. Assist in the preparation of and participate in technical reviews of projects, organizing data, and creating necessary documentation.
5. Independently conduct smaller approved projects, making suggestions for improvements based on current technical knowledge.
6. Contribute to the planning and execution of specific components of the development process, including product revisions or enhancements.
7. appropriate techniques and methods to complete assignments within negotiated deadlines, following general instructions.
8. Demonstrate a working knowledge of basic technical theories and principles within your area of expertise for routine tasks.
9. Develop an understanding of GxP (Good Practice) and related regulations and guidance applicable to the Medical Device Industry.

Skills Requirements:

1. Ability to collaborate with different stakeholders, including teams located in various locations.
2. Strong multitasking skills to work efficiently under pressure and meet project deadlines.
3. Proficiency in using software tools such as Minitab (or other statistical tools), CAD (Computer-Aided Design), and Microsoft Project.
4. Familiarity with ISO/ASTM standards related to medical devices (e.g., ISO80369, ISO 8536, etc.).

Education & Work Experience:

• 2-3 years of relevant experience in Research and Development within the Medical Device Industry.
• Bachelor's Degree in Engineering or a related field from an accredited university.