Software Quality Engr II

Location: 250 Medtronic Dr Bldg 1 Lafayette COLORADO United States 80026

Duration: 6 months

JOB DESCRIPTION

Top 3 technical skills that are required for the role:

Requirements Analysis and Management:
This skill is crucial for evaluating product definition requirements, ensuring that software product requirements are clear, complete, and testable, and assessing test coverage with respect to requirements and design outputs.

Software Documentation and Specification:
The ability toreview and remediate design output documentation, such as software architecture documentation and software form and behavior specifications, is key. This includes ensuring these documents meet intended use and performance criteria.

Quality Assurance and Compliance:
Knowledge and experience in quality assurance practices, especially related to following Quality System Practices and meeting FDA, ISO, and European Medical Device standards and regulations, are essential. This includes identifying design-related gaps and implementing mitigation strategies.

Education Required:Bachelor’s Degree in Engineering, Science or technical field

Years’ Experience Required
:
Bachelor’s Degree in Engineering, Science or technical field with2+ years of work experience in Engineering and/or Quality OR Advanced Degree in Engineering, Science or technical field with 0+ years of work experience in Engineering and/or Quality.

Will the contractor be working 40 hours a week? Yes 40 hours a week

Does this position require the candidate to be onsite or remote
:
Onsite

What is your timeline for scheduling interviews? As soon as possible.

What product linewill this person support? Stealth Station in Navigation business unit.

· This position has the opportunities to work withcorss-functional team members to support Post Market Software related activities:

· Post Market Release lifecycle, such as remediation, CAPA, and other activities as assigned.

· Responsibilities may include but not limited tothe following activities, with mentor/coach/guidance from more senior Software quality engineers:

· Supports product quality ensuring the implementation of cutting-edge technology for medical devices is safe,effective, and compliant with regulations, standards, and industry practices.

· Conducts evaluation of software systems activities including requirements, design, development, documentation,integration, test, verification and validation.

· Ensures that projects and process control documentation are compliant with requirements, objectives and/or contracts.

· Reviews software systems design, change specifications, and plans against process requirements.

· Collaborate with test engineering on verification and validation strategies, review and approve test protocols and reports.

Nice to Have

· Experience in the medical device industry

· Experience with FDA Quality System Regulations,Medical Device Directive, ISO 13485, ISO 14971, and ISO 62304 standards

· Navigation systems experience preferred

· Excellent oral and written communication skills

“TAJ Technologies, Inc. is an EEO/AA

Employer:

women, minorities, the disabled and veterans are encouraged to apply”