Primary Job Responsibilities:
- Developing new designs, assemblies, processes, and applications.
- Generate material and component specifications
- Generate test protocols, reports and manufacturing instructions.
- Organize and maintain R&D lab.
- Generate engineering drawings of devices and fixtures.
- Prototyping and building devices and fixtures for design evaluation and testing.
- Assisting in development of assembly and manufacturing processes.
- Testing and other design evaluation, verification and validation activities per written test procedures.
- Assist in Risk Management activities
- Inspection of components, sub-assemblies and finals assemblies for pilot builds.
Secondary Job Responsibilities:
- Communicate effectively and clearly, through verbal and written means
- Work independently with minimal supervision.
- Support product development, manufacturing and release.
- Perform other activities as necessary and as directed by Senior Management.
Minimum Education Required:
- BEngg or equivalent degree in technical area.
Additional Qualifications Required:
- Must have experience in design / product development, preferably in medical device industry.
- Previous experience in catheters and stents will be a plus.
- Experience with using 3D CAD software (e.g. SolidWorks, AutoCAD).
- Must have knowledge and competency in Electromagnetic compatibility, MRI safety, Ethylene Oxide Sterilization, and Biocompatibility.
Minimum Experience:
- 2-5 years experience in design / product development, preferably in medical device environment.
Supervisory Responsibilities:
Working Conditions:
- Office environment
- No medical conditions preventing access to the controlled production areas.
