Senior Biomechanical Engineer: Device-Skin Interface Expert

WearOptimo; Brisbane; On-site; AUD 180,000 - 240,000; Full time

Job summary

WearOptimo in Brisbane seeks a Principal Biomechanical Engineer to lead design, testing and validation of biomechanical aspects for Microwearable™ Hydration sensors. You will drive device–skin interfaces, ensure comfort and biocompatibility, and shepherd designs from concept to manufacture with cross‑functional leadership.

The role requires hands‑on expertise, a PhD in a related field and 8+ years in biomechanical/medical device engineering, plus experience with regulatory standards and

Qualifications

• Hands‑on biomechanical testing and validation for wearable devices.
• Strong experimental design and data interpretation skills.
• Experience guiding cross‑functional teams through product development.

Responsibilities

• Lead device–skin interface design for secure adhesion and comfort.
• Define biomechanical performance requirements and acceptance criteria.
• Design and conduct mechanical engagement testing and histology analysis.
• Plan on‑body hydration clinical trials and data analysis.
• Ensure biocompatibility and compliance with ISO and regulatory standards.
• Support transfer of designs to manufacturing and scale‑up.
• Coordinate with vendors, labs and partners for validation and deliverables.
• Maintain design files, test protocols and technical documentation.

Skills

Biomechanical testing

Data analysis

Statistical analysis

CAD

Finite element analysis

Cross-functional collaboration

Programming (statistical / data)

Education

Bachelor’s degree in Biomechanical, Biomedical, or Mechanical Engineering

PhD in biomechanics or biomedical engineering

Tools

Statistical software

CAD software

Job description

WearOptimo in Brisbane seeks a Principal Biomechanical Engineer to lead design, testing and validation of biomechanical aspects for Microwearable™ Hydration sensors. You will drive device–skin interfaces, ensure comfort and biocompatibility, and shepherd designs from concept to manufacture with cross‑functional leadership.

The role requires hands‑on expertise, a PhD in a related field and 8+ years in biomechanical/medical device engineering, plus experience with regulatory standards and