Medical Device Software Engineer (MS Windows Specialization) Zeltiq Aesthetics, Inc.
THIS JOB HAS EXPIRED Description
Title: Medical Device Software Engineer (MS Windows Specialization)
Reports To: Manager, Software Engineering
Department: Product Development
We are looking for an energetic and personable software professional to join our development team. The successful candidate will help design and build a medical device which includes embedded Windows, real-time microcontrollers and will interface with desktop Windows applications.
He / she will be a strong communicator, highly self-motivated, able to work well in a team environment and be comfortable working with electrical and mechanical engineers as well as marketing personnel to help develop and then implement product requirements. The person taking on this position is expected to hit the ground running by making significant individual contributions as well as starting to assume technical leadership in the short term and eventually carry a significant portion of the software product vision.
Essential Duties and Responsibilities include the following (other duties may be assigned.):
? Design and development of Windows-based embedded and desktop applications, using .NET Framework and C#.
? Work collaboratively with and provide technical leadership to internal and external resources to design and develop the Windows embedded system and PC based tools.
? Contribute to requirements definition at the functional level.
? Contribute to project planning and tracking activities, including effort estimation, scheduling, tracking, and priority-setting.
? Integrate and debug software and hardware components.
? Work with Software Test, Support and Manufacturing to resolve software issues.
? MS (or BS and equivalent experience) in Software Engineering, Electronics Engineering, Computer Science or related discipline.
? At least 12 years of software design and development experience (with at least 7 years of Windows experience) and at least 5 years of experience with embedded Windows programming with C# and . NET.
? Demonstrated technical leadership of major software development program.
? Experience in medical devices or similarly controlled software environment.
? Experience developing WPF-based applications as well as exposure to MEF and WCF strongly preferred.
? Hands-on product software design, development, deployment, and support experience, including extensive experience interfacing software and electronics.
? Experience in structured software and systems development and integration, including experience in software design methodologies, design patterns, component-oriented software architecture to produce high-quality software applications.
? Candidate should be a strong team player with the demonstrated abilities and willingness to wear ?multiple hats? and perform a wide range of tasks within a dynamic environment.
? Knowledge of software life cycle processes used in regulated development environments.
? Ability to communicate effectively with peers, management, and international customers to solve problems and broker information.
? Result-oriented, self-motivated and able to participate as both a team member and an individual contributor.
? Experience with Security Analysis and Design. Familiarity with Common Criteria (ISO/IEC 15408), PKI protocols and smart cards.
? Knowledge of wired and wireless communication interfaces for embedded systems ? modem, WiFi, LAN, USB, Serial, i2C, SPI
? Experience developing software in multi-threaded/multi-tasking environments preferred.
? Responsible for performing all duties in compliance with FDA?s Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies.
||Pleasanton, CA |
THIS JOB HAS EXPIRED