Job Title: Engineer, Research and Development
Reports To: Director, Research & Development (Devices)
Position Summary:
Miramar Labs (www.miramarlabs.com), an early commercial stage medical
device start-up located in Sunnyvale, is seeking a hands-on R&D
Engineer. In 2012 Miramar launched its first microwave based
dermatologic device in the US. Since late 2013 the R&D team has
renewed focus on development of novel devices to treat unmet needs in
dermatology.
This R&D position requires creative thinking and application of sound
engineering principles to contribute to next generation device design
and development. The candidate should be a strong individual
contributor with hands on abilities. Responsibilities will include
designing and prototyping devices which make use of machined parts,
injection molded parts and electromechanical assemblies. High
precision fixture development and software prototyping for proof of
concept will also be required. Proficiency with SolidWorks and
competency in the machine shop are necessary. The candidate will
have basic knowledge of electronics and experience with MatLab,
Labview or other programming languages.
Please submit cover letter and resume to: hr_at_miramarlabs.com
Minimum Qualifications / Required Competencies:
Proficiency in the machine shop (mill and lathe) Proficiency in
SolidWorks Knowledge of electronics and electromechanical systems
Experience with software programming
Education and/or Experience:
. BS or MS (ME degree preferred)
. Prior exposure to medical device development is a plus
Essential Functions:
. Work with engineers and technicians to complete assigned tasks and
projects including creating working prototypes, specifications, and
documentation for new products or product revisions . Complete
projects (including product enhancements) in an aggressive manner
consistent with corporate objectives . Contribute to the intellectual
property position of the company via invention and patent
applications . Maintain accurate documentation of concepts, designs,
drawings and processes . Identify and oversee outside vendors and
consultants as required . Present technical data in design review
meetings . Maintain a professional, credible image with key
physicians, consultants, vendors and co-workers . Comply with design
controls requirements for medical device development . Comply with
Miramar Labs' quality system requirements as well as any applicable
regulatory requirements . Participate in device risk analysis
activities . Comply with all health and safety regulations, policies
and work practices . Perform other duties as assigned
FLSA Status: Exempt
hr_at_miramarlabs.com
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Received on 2014-05-19 10:46:28