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Redbock - an NES Fircroft company

Reliability Engineer II

Redbock - an NES Fircroft company, Mounds View, Minnesota, United States

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Redbock - an NES Fircroft company provided pay range This range is provided by Redbock - an NES Fircroft company. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range $35.00/hr - $45.00/hr

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Reliability Engineer II (Through end of April 2027 // Mounds View, MN) Note from the Manager: 100% on site

Top 3 Skills

Reliability Engineering and Design Assurance testing, such as functional, stress, HALT/ALT, and accelerated life testing

Product Test Method Development

Product Test Method Validation and Design Verification support

Primary Responsibilities

Setup and execution of test methods for Test Method Validation or Design Verification

Report writing and approval

Custom sample and/or fixture development

Target Years of Experience: 1-3 years of product testing experience

Duties

Navigates the complexity of government and industry regulations to include 21 CFR Part 820 Quality System Regulation (QSR), ISO 13485, European Union (EU) Medical Device Regulation (MDR), ISO 14971.

Ensure Design Quality Assurance-driven initiatives meet objectives in delivering highest quality products, with supporting tools and processes.

Acts as a collaborative effective leader or team member in supporting quality disciplines, decisions, and practices.

Develop and/or support the development of risk management architecture, support Design for Reliability and Manufacturability (DRM) targets, support design and phase reviews, and support design transfer.

Develops, modifies, applies, and maintains standards for software systems quality operating methods, processes, and procedures.

Develops overall operating criteria to ensure implementation of the quality program according to project, process and contract requirements and objectives, and ensures compliance of projects and related documents with requirements and standards.

Reviews design, change specifications, and plans against contractual and/or process requirements.

Reviews include applicable specifications, materials, tools, techniques, and methodologies.

Provides or directs verification of device requirements, traceability, and testability.

Recommends and implements design or test methods for achieving required levels of product reliability.

Plans and leads test method validation of design verification methods. Responsible for design verification planning and execution. Responsible for verifying product and software performance meets design requirements.

Utilizes statistical analysis tools to analyze data, such as Analysis of Variance (ANOVA), Gage Repeatability and Reproducibility (Gage R&R), Attribute Agreement Analysis and Test Method Validation (TMV). Completes reports.

Completes risk management files of new design and updates to released products.

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

Required Experience

Bachelor's Degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality OR Advanced degree in Engineering, Science or technical field with 1+ years of work experience in Engineering and/or Quality

Reliability Testing, Design Verification, and/or Test Method Validation

Strong written and verbal communication skills and ability to work cooperatively as part of a cross-functional team

Nice To Haves

1-3 years of Medical Device industry experience

Familiar with FDA 21 CFR Part 820, EU 217/745 (EU MDR)

Familiar with these standards: ISO 13485, ISO 14971, IEC 60601

Knowledge of Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS

Seniority level Mid-Senior level

Employment type Contract

Job function Medical Equipment Manufacturing

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Benefits

Medical insurance

Vision insurance

401(k)

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