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Quality Engineer III

Talent Software Services

Maple Grove, MN

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JOB DETAILS
SALARY
$55–$60 Per Hour
JOB TYPE
Full-time, Employee
SKILLS
American Society for Quality (ASQ), Biomedical Engineering, Communication Skills, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Data Analysis, Design Verification, Documentation, Electrical Components, Electrical Engineering, Electricity, External Audit, Failure Mode and Effects Analysis (FMEA), Hazard Analysis, ISO (International Organization for Standardization), Internal Audit, International Electro-Technical Commission (IEC), Leadership, Maintain Compliance, Medical Equipment, Mentoring, Presentation/Verbal Skills, Product Development, Product Management, Quality Engineering, Quality System Requirements (QSR), Regulations, Reliability Testing, Research & Development (R&D), Risk, Risk Analysis, Risk Management, Safety Standards, Support Documentation, Technical/Engineering Design, Testing, Usability Engineering, Validation Plan, Validation Testing, Writing Skills
LOCATION
Maple Grove, MN
POSTED
3 days ago
Description:
About the role:
*** is currently recruiting for a Senior Design Assurance Engineer in our Arbor Lakes, MN location. This is an exciting opportunity to participate in the assessment, remediation, and sustaining of medical electrical equipment/systems (MEE) within Vascular Therapies (VT), which is a rapidly growing division of ***.

The Sr Design Assurance Engineer provides focused quality engineering leadership on sustaining design assurance activities. Design assurance drives the ISO14971 risk management process and the Verification & Validation (V&V) process. This includes quality plans, risk management plans and reports, hazard analysis, product risk management workbook (user FMEA and design FMEA), sampling systems / procedures and statistical techniques, verification protocols/testing/reports, validation protocols/testing/reports. This role will be responsible for supporting risk document and post market record review during remediation activities as well as ensuring quality and compliance through post commercialization sustaining activities.

Your responsibilities will include:
•Support remediation assessment teams with the evaluation of risk documentation and post market record review (PIR, CAPA, past Field Actions (as applicable)
•Lead or mentors the project team in the execution of deliverables such as Design and Development Planning, Risk Management, Design Verification, Reliability and Validation, Usability Validation plans, Design Review, Field Assessment, Design Change, and NCEP/CAPA/PIR
•Effectively communicates within project team, across functions, and elevates issues above the project team as appropriate
•Develops solutions to complex and diverse technical problems which require the regular use of ingenuity and creativity. Analysis of situations or data requires an in-depth evaluation of various factors
•Influences cross-functional plans, guides overall project strategy, knows when to solicit feedback, and facilitate project decisions
•Builds quality into all aspects of work by maintaining compliance to all quality requirements, defending work of their team, as well as supports internal external regulatory audits
•Supports functional and divisional design quality goals and priorities
What we're looking for in you:

Required qualifications:
•Bachelor's degree in mechanical, electrical, biomedical engineering, or related discipline
•5+ years of related experience in design assurance, new product development, or related medical device or regulated industry experience
•Understanding of electrical safety standards IEC 60601
•Experience with reliability testing
•Demonstrated use of Quality tools/methodologies
•Strong written/verbal communication skills.
•Risk documentation per ISO14971

Preferred qualifications:
•Experience with class III medical devices
•BS in Electrical Engineering
•Previous R&D experience
•Strong knowledge of QSR and ISO standards
•Medical device experience
•ASQ certification

About the Company

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