Position: Instrument Software Engineer

Location: Palo Alto

Reports to: VP of Engineering

FLSA Status: Exempt/Salary

Total fundraise $57ml. Most recent round $20ml.

Overture Life is for a Head of Engineering to join our growing team.

Overture Life is founded on the belief that IVF is too expensive, and results are not good enough to meet our vision of reproductive freedom meaning people should be free to choose if and when to have a family. We are fortunate to be backed by amazing investors including Khosla Ventures, Google Ventures, Overwater Ventures and more.

We are addressing this head on by automating the embryology lab - the heart of every IVF clinic to standardize and improve all processes from egg and embryo freezing and thawing to embryo making and more.

Our first product - the DaVitri automates egg freezing so it can be done outside the embryology lab. The device uses microfluidics to carefully manage the process of preparing the egg for freezing. Our other products span a range of technologies from robotics, mass spectrometry, machine vision and machine learning.

Our goal is to drive up success rates in IVF by improving every aspect of the embryology lab to allow more people to walk home with a baby after embarking on IVF.

Job Summary: We are seeking a talented Software Engineer to join our dynamic team and contribute to the development of next-generation IVF medical devices. In this role, you will be responsible for designing, developing, and maintaining the software that powers our state-of-the-art reproductive technologies. You will work closely with hardware engineers, clinical experts, and product managers to create seamless and reliable software solutions that integrate with our medical devices. As a key member of our startup, you will have the opportunity to influence product development and shape the future of IVF technology.

Key Responsibilities:

• Software Development:
• Design, develop, and maintain software applications and embedded systems for IVF medical devices.
• Implement algorithms, control systems, and user interfaces that enhance device functionality and user experience.
• Write clean, efficient, and maintainable code while adhering to best practices in software engineering.
• Integration and Testing:
• Collaborate with hardware engineers to integrate software with device hardware and ensure seamless operation.
• Develop and execute test plans, including unit tests, integration tests, and validation procedures to ensure software reliability and performance.
• Troubleshoot and debug software issues, providing timely resolutions and improvements.
• Documentation and Compliance:
• Create and maintain comprehensive software documentation, including design specifications, user manuals, and compliance reports.
• Ensure software development processes comply with FDA regulations and ISO standards for medical devices.
• Collaboration and Innovation:
• Work closely with cross-functional teams, including mechanical engineers, regulatory affairs, and clinical experts, to drive product development.
• Stay updated with the latest advancements in software technology and medical device regulations to incorporate innovative solutions into the product.

Required Qualifications:

• Education: Bachelor’s degree in Computer Science, Software Engineering, or a related field.
• Experience: Minimum of 3 years of experience in software development, with a focus on embedded systems or medical devices.
• Skills:
• Proficiency in programming languages such as C, C++, Python, or Java.
• Experience with software development for embedded systems.
• Microcontroller and RTOS Experience
• Peripherals Integration: I2C, SPI and CAN buses under the Yocto environment
• Linux Kernel Customization
• Strong understanding of software development lifecycle, including design, development, testing, and documentation.
• Knowledge of FDA regulations and ISO standards for medical devices is a plus.
• Excellent problem-solving skills and attention to detail.
• Strong communication skills and ability to work effectively in a fast-paced startup environment.

Preferred Qualifications:

• Advanced degree in Computer Science, Software Engineering, or a related field.
• 5+ years of experience in the medical device industry, specifically with IVF technologies or similar medical devices.
• Experience with software integration for medical device hardware and user interface design.
• Experience in a startup environment with a track record of taking products from concept to market.
• Knowledge of agile development methodologies and version control systems (e.g., Git).

Additional Information:

• Work Environment: Office-based
• Travel Requirements: Some flexibility to travel domestically and internationally, up to 6 weeks a year for clinical instrument testing

Benefits:

● Industry competitive pay

● Stock options in a fast growing, well-funded technology company

● Health insurance package options including PPO, vision, and dental for you and your dependents

● Paid Parental Leave

● 401(k)

● Paid Time Off