PhotoniCare is a fast-growing VC funded MedTech company with a mission to improve health outcomes using cutting edge technology.
We have developed the first FDA-cleared OCT-based imaging system, OtoSight Middle Ear Scope, for assisting diagnosis of ear infections, a condition that affects 80% of children.
The company operates with a philosophy of providing a fun, exciting and collaborative work environment for all team members.
PhotoniCare also makes dedicated efforts towards professional and personal growth of all its team.
We are looking for an engineer specializing in optical systems with experience in electronic design to join our team and lead the efforts related to development of OtoSight Middle Ear Scope optical systems that are critical to PhotoniCare’s imaging technology.
You will
- lead optical design of current and future products as part of a multidisciplinary engineering team from conception to production
- contribute to the high-level systems design of multidisciplinary products and components
- design, develop, build and test systems and products based on optical and electronic technologies.
- recommend modifications to the development of new photonic products and / or design changes that improve performance of existing products.
- review customer specifications, document requirements and develop component specifications based on requirements.
- Ensure the highest product quality through continual product design and manufacturing process enhancements.
- develop and maintain key supplier relationships for collaboration on product development.
- develop and maintain PhotoniCare intellectual property for key technologies and designs
You are
- An engineer who is achievement driven and focused on enabling customer success
- Familiar with Optical Coherence Tomography (OCT) system design
- Familiar with digital electronic system design
- Experience with Zemax or other optical simulation applications
- Experience with Solidworks or other mechanical CAD applications
- Preferred (but not required) experience with medical device development and related processes, such as :
- Risk management (ISO 13485)
- Failure Mode Effect Analysis (FMEA)
- Regulatory submissions (FDA 510(k))
- Usability Engineering (ISO 62366)
You will learn .
- How to bring a medical device from conception to production
- How the application of agile methodology allows rapid development of valuable products and features.
- How to navigate and apply regulatory requirements and processes
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