Senior Software Engineering Manager

Abbott•Alameda, CA

20h

About The Position

The Opportunity The Software Manager position is responsible for functional management of a software team focusing on signal processing algorithms for our fast-growing sensor products. This manager is responsible for leading the team to resolve difficult technical issues and for determining design directions in new technology areas. This will be accomplished through individual efforts and management of technical teams, as required. Responsible for overall system architecture of selected new product designs. Responsible for the identification of areas of technology for potential implementation into our products. Responsible for technical supervision and project management of the engineering activities. Ultimately the goal of the efforts of the Engineering Group is the evaluation, specification, design and testing of the sensor algorithm designs, and integrating the design with embedded and mobile product software designs and data processing ecosystems. This activity will be carried out in accordance with applicable US and International medical industry regulations and standards. What You'll Work On This position is responsible for staffing and maintaining the signal processing algorithm group’s high level of technical competence. Technical leader responsible for maintaining and enhancing the high level of technical competence of the engineering staff. Responsible for the development of technical project plans and schedules covering all engineering activities (Meeting all Design control and product development SOP requirements). Manage cross functional engineering teams developing new products. Solid knowledge of engineering principles. As a technical leader participate in the creation of schedules. Communicate effectively and participate in cross functional design teams. Participate in technical design reviews. Act as independent reviewer on programs in which their group is not directly involved. Responsible for utilizing and maintaining the effectiveness of the quality system. Lead the design and development of software across one or more domains under a disciplined product development process that meets FDA requirements. Evaluate new design approaches, work on software design, coding, and validating software, support verification and validation testing, and ensuring that all product development conforms to design specifications and coding standards for medical devices. Implement data processing algorithms efficiently in a programming language (C, C++, etc.) Define and implement data management and data flow in an embedded environment. Develop productive internal/external working relationships.

Requirements

Bachelor’s degree in technical field (Science, Technology, Engineering, or Mathematics) and 10 plus years of experience in software development (combination of programming-heavy coursework, school projects, freelance work and professional experience)
Strong knowledge of embedded software system design, experience in algorithm development implementation and data processing in embedded and other computing platforms
C, C++, structured software development and/or Object Modeling Design, digital data processing, debugger and ICE
Demonstrated experience in small embedded systems
Strong familiarity with current development tools such as IDEs, debuggers, unit test frameworks
Strong math aptitude and algorithm product development highly desired
Leadership experience required

Nice To Haves

Experience with software development life cycle processes is a plus
Experience testing software is a plus
Knowledge of design controls and regulations for medical device development is a plus
Knowledge of the principles of quality software engineering as described by software lifecycle development processes that are consistent with ISO, IEEE, or other FDA recognized standards is a plus
Team management experience is desired

Responsibilities

Functional management of a software team focusing on signal processing algorithms
Lead the team to resolve difficult technical issues and for determining design directions in new technology areas
Responsible for overall system architecture of selected new product designs
Responsible for the identification of areas of technology for potential implementation into our products
Responsible for technical supervision and project management of the engineering activities
Staffing and maintaining the signal processing algorithm group’s high level of technical competence
Maintaining and enhancing the high level of technical competence of the engineering staff
Responsible for the development of technical project plans and schedules covering all engineering activities
Manage cross functional engineering teams developing new products
Participate in the creation of schedules
Communicate effectively and participate in cross functional design teams
Participate in technical design reviews
Act as independent reviewer on programs in which their group is not directly involved
Responsible for utilizing and maintaining the effectiveness of the quality system
Lead the design and development of software across one or more domains under a disciplined product development process that meets FDA requirements
Evaluate new design approaches, work on software design, coding, and validating software, support verification and validation testing, and ensuring that all product development conforms to design specifications and coding standards for medical devices
Implement data processing algorithms efficiently in a programming language (C, C++, etc.)
Define and implement data management and data flow in an embedded environment
Develop productive internal/external working relationships