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Medical Device Innovation Jobs (NOW HIRING)

Shifamed

Sales Representative

Campbell, CA · On-site

ABOUT SHIFAMED Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address ...

Shifamed

Sales Representative

Campbell, CA · On-site

ABOUT SHIFAMED Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address ...

Medical Murray

R&D Quality Engineer II

Barrington, IL · On-site

$85K - $105K/yr

Position Overview If you are passionate about medical device innovation and thrive in fast-paced development environments where quality is built into every stage of the process, this opportunity is ...

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How much do medical device innovation jobs pay per hour?

As of Jul 2, 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 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.

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 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.
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:
What job categories do people searching Medical Device Innovation jobs look for? The top searched job categories for Medical Device Innovation jobs are:
Medical Device Innovation jobs near you
Infographic showing various Medical Device Innovation job openings in the United States as of June 2026, with employment types broken down into 5% As Needed, 89% Full Time, 3% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Senior Manager, Engineering Flexible Endoscopes and Charlton CoE Lead

Karl Storz GmbH & Co. KG

Charlton, MA • On-site

Other

Posted 6 days ago

Job description

About the Role

Senior Manager, Engineering - Flexible Endoscopes & Charlton CoE Lead

This role leads the KARL STORZ Development Engineering group focused on flexible endoscopic products, overseeing design, development, and lifecycle management. The position ensures high-quality product design, compliance with standards, and successful execution from concept through production, while also serving as a key liaison across R&D, production, and product management.

Key Responsibilities
  • Lead design, development, testing, and manufacturing transition of flexible endoscope products
  • Manage complex R&D projects, ensuring delivery on time and within budget
  • Oversee product improvements, upgrades, and cost reduction initiatives
  • Ensure compliance with FDA, ISO, and internal quality standards
  • Provide leadership, coaching, and development for engineering team members
  • Collaborate cross-functionally with production, technical teams, and product line management
  • Serve as Charlton CoE Lead, including oversight of electronics and sterilization leads
  • Act as site lead and audit contact for US R&D operations
  • Support risk management activities to ensure safe and compliant product releases
Requirements
  • Bachelor's degree in Mechanical Engineering (or related field)
  • 8+ years of experience in medical device product development
  • Strong proficiency in SOLIDWORKS and CAD tools
  • Experience with FDA QSR, ISO 13485 / 9001, and regulated environments
  • Proven experience leading technical teams and cross-functional projects
  • Strong project management, problem-solving, and analytical skills
Nice to Have
  • Experience leading international teams
  • Background in endoscopic or complex medical device systems
  • Advanced experience with product lifecycle documentation and audits
What You'll Need to Succeed
  • Strong leadership and team development capabilities
  • Ability to build consensus across multidisciplinary teams
  • Excellent communication and presentation skills
  • Detail-oriented with a proactive, self-directed approach
  • Ability to navigate ambiguity and drive technical decision-making
What We Offer
  • Opportunity to lead cutting-edge medical device innovation
  • Collaborative, cross-functional R&D environment
  • Exposure to global engineering teams and projects
  • Career growth within a leading MedTech organization
KARL STORZ Company Overview

KARL STORZ is a global leader in endoscopic technology, delivering innovative medical solutions that improve patient outcomes. As a family-owned company, KARL STORZ combines a legacy of precision engineering with a commitment to advancing minimally invasive care worldwide.

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