Principal Device Engineer

EdgeOne Medical -
Wheeling, IL

Apply Now

Job Details

Qualifications

Developing medical devices
Medical device validation
Content creation for technical audiences
Defect resolution root cause analysis
Accreditation standards (regulatory compliance area)
Medical device testing
ISO standards
Defect analysis
Bachelor's degree in engineering
Regulatory/legal compliance standards in production
Design controls
Biomedical regulatory compliance
Verification of laboratory test methods
Root cause analysis
Technical writing experience within technology
Test validation method
Test Planning (Quality assurance practices)

Full Job Description

Function: Engineering

Summary

Applies a solid understanding of medical device/combination product development toward the development of new products and remediation of Design History Files and testing programs. Fulfills technical lead role and creates client specific deliverables to support development or lifecycle management activities.

Please send your resume and a cover letter to [email protected] and include Principal Device Engineer in the Title.

Essential Duties and Responsibilities

Executes creation of new product development and lifecycle management deliverables for medical devices and/or combination products, including plans, product requirements and risk documentation, on time and within project budget.
Generates and/or manages development of testing documentation needed to support characterization, method development, method validation, and device design verification testing activities.
Fulfills technical lead role on multiple device development and testing project with minimal supervision.
Supervise engineers, technologists, technicians, and/or interns directly or indirectly as needed.
Proactively identifies areas of project and/or technical risk, escalates issues in an expedient manner, and actively proposes solutions.
Assures work activities are conducted in a manner compliant with all applicable regulations and industry standards.
Maintains a culture of continuous improvement while accelerating delivery of commitments

Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

Bachelor’s degree in Engineering (Biomedical or Mechanical) required.
7+ years of experience in medical device/combination product development and designing/executing design verification and test method validations.
Familiarity with ISO 14971:2007, 13485:2016, and 21CFR820 required.
Strong time management, technical writing, and communication skills are required.
Highly motivated self-starter who can work with minimal supervision or as part of team.
Ability to problem solve and identify root causes as part of investigations.
Working knowledge of MiniTab and Microsoft Project is strongly preferred.
Familiarity with ISO 11040-4, 11040-8 and 11608-1, -2 and -3 preferred.
Manage internal and external relationships.

Equal Employment Opportunity

Discrimination in hiring, promotion and all other employment decisions on the basis of race, color, religion, gender, national origin, age, disability, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other basis protected by Federal, state or local laws is prohibited.

Apply Now

Function: Engineering

Qualifications

Equal Employment Opportunity

Job Seeker Tools

Employer Tools

Browse

Stay Connected