1. Position Title: FPGA engineer
2. Length of Contract: 6 months
3. Location/Site: Pleasanton, CA - 100% Onsite - might be flexible for remote 1 day week.
4. What are the top 3-5 skills, experience or education required for this position:
• The engineer will have a technical leadership role for designing and testing FPGA functions
• He or she develops a thorough understanding of design requirements to ensure that the system's objectives are properly defined and ultimately achieved
Job highlights
Qualifications
• BS in Electrical Engineering, Software Engineering or equivalent degree
• Must have at least eight years of FPGA design and development experience; prefer ten years of experience
• Prefer at least three years of experience in medical devices, ideally class II devices
• Individual will complete work with minimal supervision of the manager
• Ability to set medium term project goals and outline schedules for multiple tasks for several team members
• Strong team player with the demonstrated abilities and willingness to wear "multiple hats" and perform a wide range of tasks within a dynamic environment
• Individual must have strong verbal and written communication skills
• 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
Responsibilities
• The FPGA Engineer will work collaboratively with a team to design and develop medical products from initial concept through the transfer to production
• The engineer will have a technical leadership role for designing and testing FPGA functions
• He or she develops a thorough understanding of design requirements to ensure that the system's objectives are properly defined and ultimately achieved
• Essential Duties and Responsibilities include the following (other duties may be assigned.):
• Act as a technical lead for product development projects
• Provide mentoring and guidance to other team members
• Outline and execute to short-term goals to achieve overall project milestones
• Prepare, present, and document designs at technical reviews
• Refine and develop selected concept(s) with little guidance from manager
• Plan, perform, and document verification testing
• Coordinate testing by other team members,
• Help develop assembly procedures and assist in transfer methods to manufacturing
• Document ECO changes within the Document Control system
• Coordinate design tasks for other team members for complex product designs
• Coordinate design constraints within R&D groups
• Resolve any design conflicts with preferably no managerial intervention
• Will typically be the technical leader
• Proficient with basic standard concepts and constraints involved in creating new product designs
Job Description
The FPGA Engineer will work collaboratively with a team to design and develop medical products from initial concept through the transfer to production. The engineer will have a technical leadership role for designing and testing FPGA of the overall system product. Skills in FPGA are required. He or she develops a thorough understanding of design requirements to ensure that the system's objectives are properly defined and ultimately achieved.
Essential Duties and Responsibilities include the following (other duties may be assigned.):
• Familiar with Xilinx tools: Vivado and Vitis
• Familiar with: Artix7 (or similar not to box in too much)
• Familiar with: Microblaze embedded core, and C programs
• Familiar with troubleshooting
• Familiar with FPGA HLS and combining with C
• Hands on with FPGA
• Familiar with porting FPGA to FPGA
• Familiar with port FPGA to microcontrollers
• Familiar with ST Micro
• Familiar with Python
• Familiar with Xilinx build processes
• Act as a technical lead for product development projects. Provide mentoring and guidance to other team members.
• Outline and execute to short-term goals to achieve overall project milestones
• Prepare, present, and document designs at technical reviews.
Qualifications and Additional Requirements:
• 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.
EEO:
"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."