Device Software Engineer
Company: Disability Solutions
Posted on: March 12, 2023
The individual works within cross-functional teams and provides
software requirements, design and implementation for current and
next generation software and systems projects. He or she develops a
thorough understanding of design requirements to ensure that the
system's objectives are properly defined and ultimately achieved.
This role is focused on Windows development. This individual must
have strong technical skills complemented by great communications
and teamwork qualities. Experience in a software development
background in a structured/regulated environment such as medical
device development is required. Essential Duties and
Responsibilities include the following (other duties may be
- Design, develop, and support embedded, Windows desktop
- Maintain and improve released software products.
- Contribute to requirements definition at the functional
- Participate in software work product reviews/inspections.
- Interface, integrate, troubleshoot and debug software and
- Generate required product development documentation including
Functional Specifications and design documents.
- Execute manual or automated tests for verification and
validation of software applications.
- Design, code and validate software tools for use in the
manufacturing of the product.
- Work with Software Test, Support and Manufacturing to resolve
- Drive improvements to product and process quality.
- BS in Software Engineering, Electronics Engineering, Computer
Science or related discipline orequivalent combination of education
- At least 3 years of software design and development working
experience with Windows programming with C# and . NET. GUI
development experience is preferred.
- Experience in medical devices or similarly controlled software
- Experience in developing event driven, multi-threaded
Windows-based applications using .NET Framework and C#
- Must have 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.
- Knowledge of software life cycle processes used in regulated
development environments. Agile process is preferred.
- Result-oriented, self-motivated and able to participate as both
a team member and an individual contributor.
- Willing to learn new technologies and wear multiple hats.
- Experience in Windows Wix Toolset /Microsoft msi package
building and deployment is a plus
- Prior working experience with Azure or AWS is a plus.
- Knowledge of wired and wireless communication interfaces for
embedded systems - modem, WiFi, LAN, USB, Serial 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. Language and Verbal
Skills: Ability to read, analyze, and interpret engineering
specifications, general business periodicals, professional
journals, technical procedures, or governmental regulations.
Ability to write reports, specifications, business correspondence,
and procedure manuals in English. Ability to effectively present
information and respond to questions from groups of managers,
clients, and customers. Ability to clearly and concisely convey
project accomplishments, obstacles, issues, and project status.
Math Skills: Ability to define problems, collect data, establish
facts, and draw valid conclusions. Ability to interpret an
extensive variety of technical instructions in complicated,
advanced engineering or mathematical formats. Analytical and
Reading Skills: Ability to define problems, collect data, establish
facts, and draw valid conclusions. Ability to analyze a variety of
technical instructions in mathematical or diagram form and
interpret various abstract and concrete variables. Ability to read
technical and clinical literature and documents and extract
important concepts. Physical Requirements: The physical demands and
work environment described here are representative of those an
employee encounters while performing the essential functions of
this job. Reasonable accommodations may be made to enable
individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly
required to sit, stand, walk, talk and hear; up to 8 hours per day.
The employee is regularly required to lift and carry up to 10
pounds and occasionally lift and carry up to 25 pounds.Duties also
involve daily keyboard data entry. Specific vision abilities
required by this job include close vision. Work Environment: Most
work is performed in an office-like setting. The noise level in the
environment is usually low to moderate Requires regular presence in
a (clinical or engineering or animal) laboratory setting where
protective equipment or other health and safety measures and
training are required to protect against chemical, biological or
other hazards.. Noise levels may be moderate to high. Safety:
ZELTIQ is committed to the health and safety of our employees. We
expect that all employees will perform their responsibilities while
maintaining a safe, cooperative, and productive work environment,
thus ensuring the health and safety of themselves and others.
Applicable to California Applicants Only--- The below range is the
range that we in good faith believe is the range of possible
compensation for this role at the time of this posting. We may
ultimately pay more or less than the posted range and this range is
only applicable for jobs to be performed in California.This range
may be modified in the future.--- The salary range is (minimum: $
96,000 to maximum: $ 188,000)--- This job is eligible to
participate in our short-term incentive program--- This job is
eligible to participate in our long-term incentive programs--- We
offer comprehensive package of benefits including paid time off
(vacation, holidays, sick), medical/dental/vision insurance and
401(k) to eligible employees.
- Note: No amount of pay is considered to be wages or
compensation until such amount is earned, vested, and determinable.
The amount and availability of any bonus, commission, incentive,
benefits, or any other form of compensation and benefits that are
allocable to a particular employee remains in the Company's sole
discretion unless and until paid and may be modified at the
Company's sole discretion, consistent with the law.AbbVie is an
equal opportunity employer including disability/vets. It is
AbbVie's policy to employ qualified persons of the greatest ability
without discrimination against any employee or applicant for
employment because of race, color, religion, national origin, age,
sex (including pregnancy), physical or mental disability, medical
condition, genetic information, gender identity or expression,
sexual orientation, marital status, status as a disabled veteran,
recently separated veteran, Armed Forces service medal veteran or
active duty wartime or campaign badge veteran or a person's
relationship or association with a protected veteran, including
spouses and other family members, or any other protected group
status. We will take affirmative action to employ and advance in
employment qualified minorities, women, individuals with a
disability, disabled veterans, recently separated veterans, Armed
Forces service medal veterans or active-duty wartime or campaign
badge veterans. The Affirmative Action Plan is available for
viewing in the Human Resources office during regular business
hours.Significant Work Activities: N/ATravel: Yes, 5 % of the
TimeJob Type: ExperiencedSchedule: Full-timeCompensationMinimum
Salary $96,000 Maximum Salary $188,000
Keywords: Disability Solutions, Pleasanton , Device Software Engineer, IT / Software / Systems , Pleasanton, California
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