Bachelor's degree in Biomedical engineering, or equivalent Minimum 2-4 years related working experience, or equivalent Experience working within a quality management system and quality system controls (e.g. Design inputs/outputs, Verification/validation, etc.) Knowledge of the design requirements as per 21 CFR 820 and ISO 13485 Candidates should be self-starters and have a hands-on approach Ability to work independently and within a diverse group of Engineers Strong communication skills (verbal/written) Bachelor's degree in Biomedical, Mechanical, or Electrical Engineering preferred Experience working within medical device R&D departments, with hands-on prototyping and testing Familiarity with industry related standards (e.g. ISO, ASTM, ASME, IEC, etc.) and their application Experience with product lifecycle management Experience with catheter devices development Experience with injection molding component design Experience with electrical medical device testing and development