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Contract Medical Device Design Jobs in Arizona (NOW HIRING)

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

... medical device design principles while preparing students for biomedical engineering coursework ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

Sr. R&D Engineer

Scottsdale, AZ

$105K - $144K/yr

Essential Duties and Responsibilities: · Lead development of advanced medical device reprocessing solutions in compliance with design controls and applicable FDA and ISO requirements. · Design ...

Sr. R&D Engineer

Scottsdale, AZ · On-site

$101K - $139K/yr

Essential Duties and Responsibilities: • Lead development of advanced medical device reprocessing solutions in compliance with design controls and applicable FDA and ISO requirements. • Design ...

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Contract Medical Device Design information

What is the difference between Contract Medical Device Design vs Medical Device Design Engineer?

AspectContract Medical Device DesignMedical Device Design Engineer
CredentialsTypically requires a degree in engineering or related field; certifications like ISO 13485 are a plusRequires a degree in biomedical, mechanical, or electrical engineering; professional certifications may enhance prospects
Work EnvironmentProject-based, often freelance or consulting; varies by client and project scopeFull-time employment within a company or R&D department
Employer & Industry UsageUsed by consulting firms, contract agencies, and medical device startupsEmployed by medical device companies, hospitals, or research institutions

Contract Medical Device Design professionals focus on project-specific work, often freelance, while Medical Device Design Engineers are typically employed full-time within organizations. Both roles require similar technical credentials but differ in work setting and employment structure.

What are the most commonly searched types of Medical Device Design jobs in Arizona?

The most popular types of Medical Device Design jobs in Arizona are:

What cities in Arizona are hiring for Contract Medical Device Design jobs?

Cities in Arizona with the most Contract Medical Device Design job openings:

R&D Advanced Therapeutics Manager- Relocation Assistance Provided

Innovative Health LLC

Scottsdale, AZ • On-site

Full-time

Posted 15 days ago


Job description

The R&D Advanced Therapeutics Manager role is responsible for leading the development of advanced medical device reprocessing platforms, including Class III devices and complex electromechanical systems. This role provides both strategic and hands-on leadership across advanced therapeutic device reverse engineering and process development, with a focus on system-level architecture, disassembly/reassembly processes, component replacement strategies, and validation of functional equivalence.Essential Duties and Responsibilities:Strategic & Technical LeadershipDefine system-level architecture across different therapeutics platforms.Establish engineering requirements framework in compliance with FDA, ISO, and internal design controls.Define electrical performance criteria, functional equivalence requirements, and acceptance criteria for reprocessed devices.Lead cross-platform engineering strategy to ensure reuse of validation frameworks.Advanced Reprocessing DevelopmentDevelop and implement disassembly, component replacement, and reassembly strategies for complex devices.Lead reverse engineering and second-life device design approaches.Define critical-to-function components and replacement thresholds.Validation & Test ArchitectureBuild validation architecture covering: Electrical performanceMechanical performanceSystem-level functional equivalenceOversee development of test methods, protocols, and design verification and validation strategies.Program ExecutionLead R&D programs from concept through production.Manage timelines, technical risk, and resource allocation.Partner with RA/QA to define regulatory pathways and validation expectations.Team DevelopmentLead, mentor, and develop engineering team (Sr Engineers, Engineers, Technicians).Support hiring strategy aligned with technical roadmap.Foster a collaborative, high-performance culture. Supervisory Responsibilities:· Direct supervision of R&D engineering team members· Responsible for hiring, coaching, and performance managementEducation, Qualifications and Skills:· Bachelor's degree in engineering (Electrical, Mechanical, Biomedical or related); advanced degree preferred· 8 – 10+ years of experience in medical device R&D· Strong experience in Class III medical device development· Experience with system-level architecture and electromechanical systems· Deep understanding of design controls, risk management, and validation for FDA-regulated products· Strong leadership, problem-solving, and communication skills· Ability to work in a fast-paced, collaborative environment