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Medical Device Innovation Jobs (NOW HIRING)

Medical Device Assembler

Arvada, CO ยท On-site

$19.50 - $21/hr

Our relentless commitment to patients and strong legacy of innovation in healthcare are the ... LivaNova is a global medical technology company built on nearly five decades of experience and a ...

Medical Device Assembler

Arvada, CO ยท On-site

$19.50 - $21/hr

Our relentless commitment to patients and strong legacy of innovation in healthcare are the ... LivaNova is a global medical technology company built on nearly five decades of experience and a ...

Our relentless commitment to patients and strong legacy of innovation in healthcare are the ... LivaNova is a global medical technology company built on nearly five decades of experience and a ...

Medical Device Assembler

Tucson, AZ ยท On-site

$19 - $20.61/hr

Job Title - Assembler - 3rd Shift Location - 1910 East Innovation Park Drive, Tucson, AZ, USA, 85755 Duration - 12 months contract (possibility of extension) Pay Rate - $20.61 USD hourly on W2 Work ...

Be Seen First

... preferably medical device) * Confident presence and strong influencing skills; excellent ... Strong sense of creativity and innovation * Proven track record of consistently meeting and/or ...

Be Seen First

... preferably medical device) * Confident presence and strong influencing skills; excellent ... Strong sense of creativity and innovation * Proven track record of consistently meeting and/or ...

Be part of a highly experienced leadership team with a strong track record in medical device innovation. * Make a direct impact on product quality, manufacturability, production capacity, and patient ...

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Medical Device Innovation information

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$21

$49

$96

How much do medical device innovation jobs pay per hour?

As of May 28, 2026, the average hourly pay for medical device innovation in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Innovation, and why are they important?

To thrive in Medical Device Innovation, you need a strong background in biomedical engineering or related fields, knowledge of regulatory standards, and experience with product development. Familiarity with CAD software, prototyping tools, and regulatory approval processes such as FDA or CE marking is typically required. Creativity, problem-solving, and effective cross-functional communication are standout soft skills in this role. These competencies are essential for designing safe, effective devices that meet market needs and comply with stringent regulations.

What are some common challenges faced by professionals working in Medical Device Innovation, and how can they be addressed?

Professionals in Medical Device Innovation often encounter challenges such as navigating complex regulatory requirements, ensuring cross-functional collaboration, and balancing innovation with patient safety. Staying up-to-date with regulatory changes and fostering open communication among engineering, clinical, and regulatory teams are essential for success. Additionally, adopting agile development methodologies and engaging with end-users early in the design process can help address these challenges and lead to more effective, compliant products.

What is medical device innovation?

Medical device innovation refers to the development and improvement of medical instruments, equipment, and technologies used in healthcare to diagnose, treat, or monitor patients. This process involves research, design, prototyping, regulatory approval, and commercialization of new or enhanced medical devices. The goal is to address unmet medical needs, improve patient outcomes, and increase the efficiency of healthcare delivery. Professionals in this field work closely with clinicians, engineers, and regulatory bodies to ensure devices are safe, effective, and compliant with industry standards.

What is the difference between Medical Device Innovation vs Medical Device Regulatory Affairs?

AspectMedical Device InnovationMedical Device Regulatory Affairs
Primary FocusDeveloping new medical devices, product design, and technological advancementsEnsuring compliance with regulations, managing submissions, and maintaining approval processes
Required CredentialsEngineering, product development, or biomedical backgroundsRegulatory affairs certifications, healthcare law knowledge
Work EnvironmentResearch labs, product development teams, innovation hubsRegulatory agencies, corporate compliance departments
Industry UsageDesign and create innovative medical devicesNavigate regulatory pathways and ensure legal compliance

Medical Device Innovation focuses on creating and developing new medical devices, emphasizing engineering and product design. In contrast, Medical Device Regulatory Affairs concentrates on ensuring that devices meet legal and safety standards, managing approval processes. Both roles are essential in the medical device industry but serve different functions in bringing a product from concept to market.

More about Medical Device Innovation jobs
What cities are hiring for Medical Device Innovation jobs? Cities with the most Medical Device Innovation job openings:
What states have the most Medical Device Innovation jobs? States with the most job openings for Medical Device Innovation jobs include:
Infographic showing various Medical Device Innovation job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 12% Full Time, 84% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Hybrid job distribution, with an average salary of $103,662 per year, or $49.8 per hour.
Senior Oncology/Medical Technology Engineer

Senior Oncology/Medical Technology Engineer

Sd Solutions LLC

Washington, DC โ€ข On-site

$118.40K - $162.50K/yr

Full-time

Posted 19 days ago


Job description

Position Description

We are seeking an experienced scientific professional with a background in medical device innovation-spanning both hardware and software-and deep familiarity with oncology-related disciplines. Qualified candidates will have a minimum of eight years of industry experience in areas such as cancer biology, biomedical engineering, biochemistry, or related fields. This role supports a high-impact health research organization focused on advancing transformative solutions to critical public health challenges.

Key Responsibilities

In collaboration with program leadership and interdisciplinary teams, the selected candidate will help drive forward advanced research and development initiatives. Responsibilities include both technical and programmatic contributions to ensure successful execution of complex projects.

Core duties include:

  • Providing strategic and technical guidance to program leadership to support the advancement of both emerging and ongoing initiatives.
  • Evaluating the current scientific and technological landscape to identify unmet needs, research gaps, and opportunities for innovation aligned with organizational priorities.
  • Tracking and assessing project performance against defined objectives and milestones.
  • Translating complex scientific concepts into clear, concise materials suitable for diverse audiences, including senior leadership.
  • Applying rigorous analytical thinking to assess technical data, research findings, and program outputs.
  • Working both independently and collaboratively within a multi-disciplinary environment to support ongoing research efforts.
  • Preparing internal reports, summaries, and briefings based on collected and analyzed data related to health-focused programs.
  • Participating in occasional domestic travel (approximately 10โ€“20%) to support program activities and stakeholder engagement.

Required Qualifications

  • Doctoral degree (PhD) in a biomedical or engineering discipline, such as oncology, cell biology, biochemistry, biomedical engineering, chemical engineering, or mechanical engineering.
  • At least eight years of professional experience in industry settings (e.g., biotech, pharmaceutical, diagnostics), with exposure to product development environments such as startups or mid-sized companies.
  • Familiarity with regulatory considerations in diagnostics or medical device development.
  • Advanced proficiency in presentation and data analysis tools, particularly PowerPoint and Excel, including the ability to work efficiently under time constraints.
  • Excellent written and verbal communication skills.
  • Demonstrated intellectual curiosity, self-motivation, and strong task focus.
  • Eligibility to obtain a U.S. government Public Trust clearance.

Preferred Qualifications

  • Background in both basic and applied research environments.
  • Experience supporting senior leadership overseeing large-scale research programs or funding portfolios.