Sr Design Assurance Engineer - Arbor Lakes, Minnesota - Onsite

Position:

Sr Design Assurance Engineer location: Arbor Lakes, Minnesota -

Onsite Contract:

12+ months

Job Description:

We are currently recruiting 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 our Client. 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 Manoj Prajapati | Non-IT Recruiter An -

E Verified Company E:

P:

+1