Senior Staff Engineer- Med Device at Jobot
Andover, MA 01810
About the Job
This Jobot Job is hosted by: Angela Trudeau
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $150,000 - $175,000 per year
A bit about us:
We manufacture medical and safety technology products that protect, support, and save lives worldwide. Our solutions are used in hospitals, fire departments, emergency services, government agencies, mining, and various industries. With a global presence, we have over 16,000 employees and operate in more than 190 countries.
Our products are used across the globe, and we maintain operations in around 50 countries, with local sales and service teams directly supporting our customers on-site.
Why join us?
Excellent Health Benefits
Generous PTO package
Hybrid
Bonus
state of the art facility
Job Details
The candidate will be involved in designing, developing, testing, and supporting the next generation of patient monitoring systems. They will work closely with a diverse team of engineers across different disciplines in a fast-paced environment. The ideal candidate will contribute to all stages of the project, from architecture and design to implementation, and must have excellent communication skills.
Responsibilities:
Use advanced methods to develop software systems and improve existing designs.
Apply software configuration management principles, including lifecycle and maintainability practices.
Work in multidisciplinary teams to solve complex problems, often collaborating with other engineers.
Evaluate the feasibility of new projects, systems, or approaches.
Gather requirements, specification documents, and execute unit tests for software validation.
Provide technical support for research, design, development, integration, and testing.
Develop product use cases, storyboards, and user interaction flows.
Build software architecture and code to support user interfaces.
Support usability testing and work with customers to refine user interfaces.
Help debug and improve the reliability of existing designs.
Follow Design Control SOPs and adhere to the software development lifecycle.
Collaborate with Quality Assurance to meet GMP, FDA QSR, IEC 62304, ISO 9001, and other relevant standards.
Qualifications:
BS in Software Engineering, Electrical Engineering, or a related field.
6+ years of experience in software development
a master’s degree is a huge plus!
Ability to understand software requirements and work with functional teams and work across teams to implement software in accordance to standards.
Experience in all phases of the software development lifecycle.
Proficiency C++.
Experience in developing medical devices.
Strong analytical and design skills.
Familiarity with project lifecycles, software development environments, and source control techniques.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $150,000 - $175,000 per year
A bit about us:
We manufacture medical and safety technology products that protect, support, and save lives worldwide. Our solutions are used in hospitals, fire departments, emergency services, government agencies, mining, and various industries. With a global presence, we have over 16,000 employees and operate in more than 190 countries.
Our products are used across the globe, and we maintain operations in around 50 countries, with local sales and service teams directly supporting our customers on-site.
Why join us?
Excellent Health Benefits
Generous PTO package
Hybrid
Bonus
state of the art facility
Job Details
The candidate will be involved in designing, developing, testing, and supporting the next generation of patient monitoring systems. They will work closely with a diverse team of engineers across different disciplines in a fast-paced environment. The ideal candidate will contribute to all stages of the project, from architecture and design to implementation, and must have excellent communication skills.
Responsibilities:
Use advanced methods to develop software systems and improve existing designs.
Apply software configuration management principles, including lifecycle and maintainability practices.
Work in multidisciplinary teams to solve complex problems, often collaborating with other engineers.
Evaluate the feasibility of new projects, systems, or approaches.
Gather requirements, specification documents, and execute unit tests for software validation.
Provide technical support for research, design, development, integration, and testing.
Develop product use cases, storyboards, and user interaction flows.
Build software architecture and code to support user interfaces.
Support usability testing and work with customers to refine user interfaces.
Help debug and improve the reliability of existing designs.
Follow Design Control SOPs and adhere to the software development lifecycle.
Collaborate with Quality Assurance to meet GMP, FDA QSR, IEC 62304, ISO 9001, and other relevant standards.
Qualifications:
BS in Software Engineering, Electrical Engineering, or a related field.
6+ years of experience in software development
a master’s degree is a huge plus!
Ability to understand software requirements and work with functional teams and work across teams to implement software in accordance to standards.
Experience in all phases of the software development lifecycle.
Proficiency C++.
Experience in developing medical devices.
Strong analytical and design skills.
Familiarity with project lifecycles, software development environments, and source control techniques.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
150,000 - 175,000 /year