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Medical Device Research And Development Jobs (NOW HIRING)

Conduct research, data analysis, and benchmarking to support client engagements in pharmaceutical, biotech, and medical device R&D * Assist in developing recommendations for process improvements ...

Director of R&D - Medical Devices New Hope, MN Full-Time | $150,000-$200,000 + Bonus + Stock Options A leading medical device company in the Twin Cities is seeking a Director of Research ...

OrthoCor Medical, a division of Caerus Corp, is a rapidly growing medical device company. We are ... We are seeking a dedicated Research & Development Engineer to join our Research & Development team.

DEKA R&D, on behalf of Millyard Advanced Medical Products, is looking for a Junior Product Complaints Engineer to work in a dynamic Medical Device Research and Development environment. The position ...

OrthoCor Medical, a division of Caerus Corp, is a rapidly growing medical device company. We are ... We are seeking a dedicated Research & Development Engineer to join our Research & Development team.

Partner with Quality, Regulatory Affairs, Manufacturing, and R&D teams throughout the product ... Experience supporting medical device development or work within a highly regulated industry.

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Medical Device Assembler * Shift: Monday-Thursday, 5:00 AM - 3:30 PM (4/10 schedule) * Pay: $22-25 ... Research.

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Ability to research devices, categories, and HCPCS codes leading to the development of a library ... FDB is the leading provider of drug and medical device knowledge that helps healthcare ...

Showing results 41-60

Medical Device Research And Development information

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$48.5K

$101.8K

$165K

How much do medical device research and development jobs pay per year?

As of Aug 9, 2026, the average yearly pay for medical device research and development in the United States is $101,794.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $116,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device research and development, and why are they important?

To thrive in Medical Device Research and Development, you need a solid background in engineering or life sciences, along with experience in product design and knowledge of regulatory standards. Familiarity with CAD software, prototyping tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong problem-solving skills, creativity, and effective teamwork set standout professionals apart in this field. These skills and qualities are crucial to ensure innovative, safe, and compliant medical devices that meet both clinical needs and regulatory requirements.

What are some typical challenges faced by professionals in medical device research and development, and how can these be managed?

Professionals in Medical Device Research and Development often encounter challenges such as navigating complex regulatory requirements, balancing innovation with safety, and coordinating cross-functional teams. Managing these challenges involves staying current with FDA and international regulations, fostering open communication between engineering, clinical, and regulatory teams, and maintaining rigorous documentation throughout the development process. Strong project management skills and a collaborative mindset are key to overcoming these obstacles and ensuring successful product development.

What is medical device research and development?

Medical device research and development (R&D) is the process of designing, creating, testing, and improving medical devices used for diagnosing, treating, or preventing health conditions. This field combines engineering, biology, and medicine to develop innovative tools ranging from simple instruments to complex implantable devices. Professionals in this area work on everything from concept development and prototyping to clinical trials and regulatory approval. Their work ensures that medical devices are safe, effective, and meet strict regulatory standards before reaching patients.

What is the difference between Medical Device Research And Development vs Medical Device Quality Assurance?

AspectMedical Device Research And DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications in R&DQuality certifications, regulatory training
Work EnvironmentLabs, design teams, product developmentInspection facilities, compliance departments
Employer & Industry UsageManufacturers, biotech firms, innovation labsRegulatory agencies, manufacturing companies
Search & Comparison IntentInnovation, product development, prototypingCompliance, testing, product validation

Medical Device Research And Development focuses on designing and developing new medical devices, emphasizing innovation and prototyping. In contrast, Medical Device Quality Assurance ensures products meet safety and regulatory standards through testing and compliance. Both roles are essential in the medical device industry but serve different stages of the product lifecycle.

More about Medical Device Research And Development jobs
What cities are hiring for Medical Device Research And Development jobs? Cities with the most Medical Device Research And Development job openings:
What states have the most Medical Device Research And Development jobs? States with the most job openings for Medical Device Research And Development jobs include:
Infographic showing various Medical Device Research And Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $101,794 per year, or $48.9 per hour.

R&D Advanced Therapeutics Manager- Relocation Assistance Provided

Innovative Health LLC

Scottsdale, AZ • On-site

Full-time

Posted 4 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