R&D Engineer Project Manager
********LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO Santa Clara, CA ****NO C2C CANDIDATES*************
Requisition Title: R&D Engineer Project Manager
Location: Santa Clara, CA (Onsite)
JP# 44095
Pay Rate : 50k/Ann-70k/Ann
Description: Non-Exempt
Years Experience: 3-6 yrs in a FDA regulated industry.
Skills / Responsibilities:
1. Experience/familiar with supplier process validation and FDA regulations (ISO 9001 and 13485).
2. Comprehensive knowledge of medical device design controls and Quality Management Systems.
3. Experience with design and implementation of Project Development Plans including scope, scheduling, and resourcing.
4. Lead Meetings with external suppliers and internal cross functional teams and Keep/distribute meeting notes capturing key discussion points/decisions made/action items.
5. Drive teams to meet milestones and deliverables established in project planning and agreed upon with senior leadership.
6. Recognize and integrate the broader implications of actions and proposals on the final project outcomes.
7. Accountable for clearly defining and managing total project scope; develop and manage project charter and project plan to meet deliverables. Identify key milestones for project status reporting; complete projects on time and within budget constraints.
8. Manage creation and updates of detailed project plans, resource and budget management, schedule management, project risk assessments, and project documentation.
9. Lead cross-functional teams to execute projects, identifying tasks, creating and tracking project schedule with problem solving methodology; identify problems and work with cross-functional team to resolve them.
10. Using advanced excel skills and PowerBI, prepare and present data-informed written and oral reports and other presentations to sr. leadership audiences; under supervision, may create and deliver project review presentation to leadership as necessary.
11. Track and present budget variances, and recommend contingency options.
12. Create a work environment that supports team effectiveness
********LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO PLEASANTON, CA ****NO C2C CANDIDATES*************
Requisition Title: R&D/Software Engineer
Location: Minnesota : Pleasanton, CA (Onsite)
JP# 43953
Pay Rate : 50k/Ann-65k/Ann
Description:
This position is NonExempt. Hours over 40 will be paid at Time and a Half.
Years of Experience: 4-8 years
Education:
Bachelor or Masters in Software Engineering, Systems Engineering, Computer Science or similar field
Qualifications:
Experience -
- Med Device R&D
- Development of Application Software
- Creating/Maintaining Software Requirements
- Creating/Maintaining Software Test Cases
- Creating/Maintaining Software Test Runs
- Creating/Maintaining Software dFMEA/Risks
- Creating/Maintaining SysML (i.e. activity diagrams, use cases)
- Creating/Maintaining Trace Matrices
- Utilizing software tool for requirements, test cases
- Need mid level career engineer that is familiar with writing software requirements and software verification and validation in med device. Must have med device exp.
********LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO Twin Cities, MN ****NO C2C CANDIDATES*************
Requisition Title: Staff Software Engineer
Location: Minnesota : Twin Cities, MN (Onsite)
JP# 44115
Pay Rate : 70k/Ann- 90k/Ann
Description:
- Top 3 Required Skills: C++, Qt (including QML), OpenGL
- Top 3 Preferred Skills: Experience in medical device or defense industry; disciplined software engineering background; familiarity with regulated environments
- Certifications/Education: Minimum: Bachelor’s in Computer Science + 8 years experience; Preferred: Master’s or PhD in Computer Science
- Industry Experience: Medical or pharmaceutical preferred
- Systems Used: Linux (Red Hat), C++, Qt framework
- Personality Traits: Outspoken, self-driven, motivated, quick learner
This position works out of our Tech Center in the Twin Cities, MN in the EP division.
In client's Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.
As the Staff Software Engineer, you'll have the chance to be a critical contributor to building compelling products within Abbott’s Electrophysiology Division. The individual will participate in the development and deployment of system and software architecture to support our development programs. Design, develop, and document software applications embedded in diagnostic and interventional cardiology devices. Participate in all phases of the software lifecycle, including concept development, requirements, design, implementation, and testing.
What You’ll Work On
- Apply solid software design skills to develop medical devices to meet specific performance requirements and deliver on goals according to product development quality system. These activities include developing requirements specifications, design, implementation and testing of software and embedded software algorithms or/and general Linux applications and GUIs. These algorithms include real-time 3D location tracking, real-time 3D anatomical model creation and intracardiac signal visualization.
- As a team member, contribute significantly to completion of various project activities, from definition, identifying software functional requirements, implementation, code reviews, and final release according to medical device development processes.
- Create and implement software/test plans/protocols and generate test reports to ensure software/firmware design meets the specifications and quality system requirements.
- Work closely with cross-function team, including design reviews with QA, RA, test engineers, hardware engineers to ensure the firmware design meets the product requirements, including safety, reliability and serviceability. Be creative and innovative in the product development process.
- Make, recommend or justify critical technical decisions in product design. The decision should be based on broad investigation and testing.
- Document and transfer developed solutions to manufacturing team for mass production and provide technical support and sustaining development in launch phase.
Required Qualifications
- B.S. in Computer Science or M.S+ (Preferred) in Computer Science.
- 6+ years of software development or equivalent (e.g., 4+ years of Ph.D. research experience in Computer Science).
- 5+ years of Object-Oriented Design, C++ and Qt Programming Experiences on Linux platform.
- Strong experience in design and implementation of cutting-edge graphics techniques and detailed knowledge of graphics hardware such as OpenGL shader language, CUDA, Nvidia GPU programming, OpenGL 2D/3D texture mapping, CPU/GPU performance profiling and characterization, and other general stream programming techniques.
- Excellent knowledge and experience in computational geometry algorithms.
- Excellent knowledge and experience in developing multithreaded real-time applications.
- Excellent analytical and mathematical skills.
- Excellent interpersonal and problem-solving skills.
- Software development through full product lifecycle.
- Experience with creating and managing requirements and translating them into effective architectures and software design.
- An understanding of requirements for, and experience in medical device development.
- Excellent documentation skills (highly regulated development environment).
Preferred Qualifications
- GUI development experience: Qt/QML.