System Engineer V&V

System Engineer V&V (Hybrid) page is loaded System Engineer V&V (Hybrid) Apply locations Aviacon, Tijuana time type Full time posted on Posted 3 Days Ago job requisition id REQ Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod product platform.

In the last two decades we have improved the lives of hundreds of thousands of patients by using innovative technology that is wearable, waterproof, and lifestyle accommodating.

We are looking for highly motivated, performance driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it
Job Profile Summary


Job Title:
Systems Engineer V&V


Department:
Systems Engineering COE


FLSA Status:
Exempt

Position Overview:

The Systems Engineer V&V is a member of the Systems Engineering COE and a technical expert responsible for leading Systems Engineering activities related to verification and validation of Insulet's products.

Education and work experience should encompass a wide array of engineering disciplines relevant to:

mechanical testing, system testing, material testing, 3rd party (agency) testing, shelf life and aging testing, simulated use, and drug-device compatibility testing.

The position will report to the Manager Systems Design Verification, Systems Engineering COE, Medical Devices R&D located at Insulet's Headquarters in Acton, MA.

Responsibilities:

• Manage all Verification and Validation activities and deliverables for New Product Development and Lifecycle Project Teams.
• Develop detailed Verification and Validation Plans for assigned projects
• Develop detailed Verification schedules utilizing time based resourced management tools
• Perform detailed requirements analysis and manage Test Cases and Test Runs using RQM Tools (DOORs, Helix, Jama).
• Collaborate with Systems Engineers in Systems Engineering COE to ensure that all requirements are testable
• Participate in the planning and execution of technical project work.
• Create and document novel and robust test methodologies and provide feedback and recommendations for product/design changes
• Conduct and encourage frequent formal and informal communication with team members to ensure full engagement and efficient operation.
• Analyze design changes implemented after execution of verification and validation to determine regression testing required
• Provide technical consulting and mentoring in areas of expertise to early-career members of the Design Verification Test Team
• Manage 3rd party verification activities to ensure product is fully compliant with all applicable standards (i.e. IEC/AAMI/UL , 1-2 and applicable collateral standards)
• Develop new Test Cases and/or update existing Test Cases to match requirement updates and new understanding of system performance
• Perform dry-running of new and updated Test Cases
• Perform systemic review of Test Cases to ensure that both typical use and edge cases are properly covered (happy-path, alternate path, negative path, etc.)
• Perform and maintain product configuration management for assigned projects
• Perform verification testing following proscribed Test Cases for assigned projects.
• Other duties within the scope of the Position Overview as assigned
• Ensure compliance with Insulet quality policies, procedures and practices
• Ensure compliance with all local, state and federal regulations, policies and procures

Education and Experience:


Minimum Requirements:

• Bachelors' Degree in Biomedical Engineering, Software Engineering, Computer Science, Mechanical, Electrical Engineering or a related field.
• Minimum of 3 years' experience testing medical devices in a multidisciplinary project team environment or advanced degree and 1+ years of experience

Preferred Skills and Competencies:

• Strong technical judgement with extensive technical leadership skills
• Demonstrated capability of leading Verification & Validation Test Programs
• Excellent Program Management Skills – PMP Certification a plus
• Previous experience working in an Agile based Software Development environment strongly preferred.
• Familiarity with the story design and the use of Atlassian Tools (JIRA, Confluence, Bamboo) in the software development process.
• Experience guiding team/individuals to develop technical solutions to complex problems
• Sound knowledge of engineering first principals
• Strong Analytical and Problem-Solving Skills
• Ability to effectively and clearly communicate concepts, ideas and knowledge to other individuals and teams
• Experience in directing associates and leading small cross-functional teams
• Good written and verbal communication skills
• Familiarity with System Level Testing of software based Medical Devices
• Test Engineering training and/or certification is a plus
• Previous experience with National Instruments LabView, CVI, Test Stand and/or Measurement Studio is a big plus
• Creative out-of-the box thinker who can devise new approaches and processes that meet regulatory needs adapt to business and market needs
• Excellent project team skills; experience and capability working collaboratively under a Quality Management System (QMS), as part of a cross-functional team that includes development/verification/validation/procurement/manufacturing/regulatory and quality experts
• Demonstrated skills developing and introducing innovative FDA-regulated medical devices (Class 2 or 3) under Design Controls
• Experience with design and development processes that conform to standards such as ISO 9000, ISO 13485, IEC 62304, IEC 60601, and ISO 14971

Physical Requirements (if applicable):

• Not Applicable

Job Description


Job Title:
Systems Engineer V&V


Department:
Systems Engineering COE


FLSA Status:
Exempt

Position Overview:

Position Overview:

The Systems Engineer V&V is a member of the Systems Engineering COE and a technical expert responsible for leading Systems Engineering activities related to verification and validation of Insulet's products.

Education and work experience should encompass a wide array of engineering disciplines relevant to:

mechanical testing, system testing, material testing, 3rd party (agency) testing, shelf life and aging testing, simulated use, and drug-device compatibility testing.

The position will report to the Manager Systems Design Verification, Systems Engineering COE, Medical Devices R&D located at Insulet's Headquarters in Acton, MA.

Responsibilities:
Manage all Verification and Validation activities and deliverables for New Product Development and Lifecycle Project Teams.

Develop detailed Verification and Validation Plans for assigned projectsDevelop detailed Verification schedules utilizing time based resourced management toolsPerform detailed requirements analysis and manage Test Cases and Test Runs using RQM Tools (DOORs, Helix, Jama).Collaborate with Systems Engineering in Systems Engineering COE to ensure that all requirements are testableParticipate in the planning and execution of technical project work.

Create and document novel and robust test methodologies and provide feedback and recommendations for product/design changesConduct and encourage frequent formal and informal communication with team members to ensure full engagement and efficient operation.

Analyze design changes implemented after execution of verification and validation to determine regression testing requiredProvide technical consulting and mentoring in areas of expertise to early-career members of the Design Verification Test TeamManage 3rd party verification activities to ensure product is fully compliant with all applicable standards (i.e.

IEC/AAMI/UL , 1-2 and applicable collateral standards)Develop new Test Cases and/or update existing Test Cases to match requirement updates and new understanding of system performancePerform dry-running of new and updated Test CasesPerform systemic review of Test Cases to ensure that both typical use and edge cases are properly covered (happy-path, alternate path, negative path, etc.)Perform and maintain product configuration management for assigned projectsPerform verification testing following proscribed Test Cases for assigned projects.

Other duties within the scope of the Position Overview as assignedEnsure compliance with Insulet quality policies, procedures and practicesEnsure compliance with all local, state and federal regulations, policies and procures

Education and Experience:


Minimum Requirements:
Bachelors' Degree in Biomedical Engineering, Software Engineering, Computer Science, Mechanical, Electrical Engineering or a related field.

Minimum of 3 years' experience testing medical devices in a multidisciplinary project team environment or advanced degree and 1+ years of experience

Preferred Skills and Competencies:

Strong technical judgement with extensive technical leadership skillsDemonstrated capability of leading Verification & Validation Test ProgramsExcellent Program Management Skills – PMP Certification a plusPrevious experience working in an Agile based Software Development environment strongly preferred.

Familiarity with the story design and the use of Atlassian Tools (JIRA, Confluence, Bamboo) in the software development process.
Experience guiding team/individuals to develop technical solutions to complex problemsSound knowledge of engineering first principalsStrong Analytical and Problem-Solving SkillsAbility to effectively and clearly communicate concepts, ideas and knowledge to other individuals and teamsExperience in directing associates and leading small cross-functional teamsGood written and verbal communication skillsFamiliarity with System Level Testing of software based Medical DevicesTest Engineering training and/or certification is a plusPrevious experience with National Instruments LabView, CVI, Test Stand and/or Measurement Studio is a big plusCreative out-of-the box thinker who can devise new approaches and processes that meet regulatory needs adapt to business and market needsExcellent project team skills; experience and capability working collaboratively under a Quality Management System (QMS), as part of a cross-functional team that includes development/verification/validation/procurement/manufacturing/regulatory and quality expertsDemonstrated skills developing and introducing innovative FDA-regulated medical devices (Class 2 or 3) under Design ControlsExperience with design and development processes that conform to standards such as ISO 9000, ISO 13485, IEC 62304, IEC 60601, and ISO 14971

Physical Requirements (if applicable):
Not Applicable

NOTE:

This position is eligible for hybrid working arrangements (requires on-site work from an Insulet office at least 1x/week; may work remotely other days).

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