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Product Development Engineer Spine Medical Device Jobs

Astura Medical

Sr. Design Engineer

Irving, TX · On-site

$75K - $90K/yr

... Spinal Hardware Products team within the R&D department. The Senior Design Engineer will be ... Strong background in medical device product development, including design, testing, and ...

FHC Company

$75/hr

... engineering; medical device industry experience preferred. * Excellent technical writing of ... Contribute to development of design input requirements and product specifications. * Originate ...

Astura Medical

Sr. Design Engineer

Irving, TX · On-site +1

$75K - $90K/yr

... Spinal Hardware Products team within the R&D department. The Senior Design Engineer will be ... Strong background in medical device product development, including design, testing, and ...

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All JobsProduct Development Engineer Spine Medical Device Jobs

Product Development Engineer Spine Medical Device information

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$39.5K

$87.9K

$132.5K

How much do product development engineer spine medical device jobs pay per year?

As of Sep 14, 2026, the average yearly pay for product development engineer spine medical device in the United States is $87,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $100,000.00 per year, depending on experience, location, and employer.

What does a product development engineer do in the spine medical device industry?

A Product Development Engineer in the spine medical device industry is responsible for designing, developing, and testing new devices and implants used in spinal surgeries. They work closely with surgeons, regulatory teams, and manufacturing to ensure products meet clinical needs, safety standards, and regulatory requirements. Their role often involves prototyping, conducting feasibility studies, and supporting the product through validation and commercialization. They also play a key part in troubleshooting and improving existing products based on feedback and technological advances.

What are the key skills and qualifications needed to thrive as a product development engineer in spine medical devices, and why are they important?

To thrive as a Product Development Engineer in Spine Medical Devices, you need a strong background in biomedical or mechanical engineering, experience with medical device design, and knowledge of relevant regulatory standards such as FDA and ISO 13485. Familiarity with CAD software (like SolidWorks or Pro/ENGINEER), finite element analysis, and prototyping tools, as well as certification in design controls or quality systems, is typically required. Exceptional problem-solving, cross-functional teamwork, and effective communication are vital soft skills for collaborating with clinicians and meeting project goals. These skills and qualifications are essential to ensure innovative, safe, and compliant spine products that address clinical needs and meet regulatory requirements.

What are the main challenges faced by a product development engineer in the spine medical device industry?

Product Development Engineers in the spine medical device sector often face the challenge of balancing innovative design with strict regulatory requirements and patient safety standards. The role requires frequent collaboration with cross-functional teams, such as surgeons, regulatory affairs, manufacturing, and quality assurance, to ensure that devices are both clinically effective and manufacturable. Keeping up with advancements in biomaterials and surgical techniques, while also adhering to timelines and budgets, can be demanding but highly rewarding. Successful engineers are adaptable, detail-oriented, and proactive in seeking feedback and iterating on designs.

What is the difference between Product Development Engineer Spine Medical Device vs Mechanical Engineer?

AspectProduct Development Engineer Spine Medical DeviceMechanical Engineer
CredentialsBachelor's or Master's in Biomedical, Mechanical, or related engineeringBachelor's or Master's in Mechanical Engineering
Work EnvironmentMedical device companies, R&D labs, regulated environmentsManufacturing, design firms, R&D labs
Industry UsageMedical device industry, specifically spine devicesBroad engineering sectors including automotive, aerospace, manufacturing

Product Development Engineer Spine Medical Device focuses on designing and developing spine-specific medical devices within regulated healthcare environments. Mechanical Engineers have a broader scope, working across various industries on mechanical systems. While both roles require engineering credentials, the medical device role emphasizes regulatory compliance and clinical considerations, making it more specialized for spine device development.

What are popular job titles related to Product Development Engineer Spine Medical Device jobs?

For Product Development Engineer Spine Medical Device jobs, the most frequently searched job titles are:

Infographic showing various Product Development Engineer Spine Medical Device 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 $87,884 per year, or $42.3 per hour.

Interventional Device Development Engineer

North Attleboro, MA • On-site

Theragenics Corp
201 - 500 employees
Learn more about Theragenics Corpexternal

$105K - $165K/yr

Full-time

Re-posted 20 days ago

Job description

Compensation: 

  • 2–5 years of experience: Starting at $105,000
  • 6–9 years of experience: Progressively higher based on experience, skills, and performance
  • 10+ years of experience: Up to $165,000


Be part of a mission that matters—join Arrotek, a Theragenics company, as a Senior Interventional Device Development Engineer and help bring innovative medical technologies from concept to commercialization. In this critical role, you'll lead the design, development, optimization, and transfer of advanced interventional medical devices, including catheter and guidewire technologies that improve patient outcomes worldwide.

Working alongside multidisciplinary engineering teams, manufacturing experts, and global clients, you'll play a key role in developing life-changing solutions that enable physicians to perform safer, less invasive procedures. If you're passionate about innovation, technical excellence, and making a meaningful impact in healthcare, this is your opportunity to help shape the future of medical technology.

Company Overview

At Theragenics, we're passionate about transforming healthcare and enhancing patient outcomes. Our commitment to innovation drives us to push the boundaries of what's possible, ensuring a brighter future for patients everywhere.

Theragenics is a leader in developing medical devices focused on minimally invasive treatments for cancer, vascular interventions, and surgical applications. Headquartered in Atlanta, Georgia, the company operates facilities in Costa Rica, Texas, and Massachusetts.

Theragenics proudly operates Arrotek, a leading medical device design and development consultancy with locations in the United States and Ireland. Arrotek specializes in pioneering minimally invasive technologies that improve lives through innovative engineering, product development, and manufacturing solutions.

Role Summary

As a Senior Interventional Device Development Engineer, you will apply advanced engineering expertise to lead the development of innovative interventional medical devices from concept through commercialization. You will serve as a technical leader across development programs, mentor junior engineers, collaborate directly with clients, and drive the successful execution of complex product and process development projects in a highly regulated environment.

Key Responsibilities
  • Lead the design and development of interventional medical devices, including catheters, guidewires, and electromechanical systems.
  • Generate innovative concepts and evaluate designs through engineering analysis, prototyping, testing, and design reviews.
  • Develop, optimize, and validate manufacturing and assembly processes, including extrusion, reflow, tipping, bonding, laser processing, and precision assembly.
  • Execute and lead Design of Experiments (DOE), feasibility studies, verification, and validation activities.
  • Conduct risk assessments, FMEA activities, and design control reviews throughout the product lifecycle.
  • Develop and maintain technical documentation including DHFs, DMRs, BOMs, drawings, protocols, and engineering reports.
  • Lead technical workstreams and support project planning, scheduling, budget management, and deliverable execution.
  • Interface directly with customers to communicate project status, technical recommendations, and development strategies.
  • Mentor and provide technical guidance to junior engineers and project team members.
  • Collaborate with Quality, Regulatory, Manufacturing, Supply Chain, and external partners to ensure successful product development and commercialization.
  • Support manufacturing transfer, process scale-up, root cause investigations, and continuous improvement initiatives.
  • Ensure compliance with FDA, ISO 13485, ISO 14971, MDR, and applicable regulatory requirements.
Qualifications & SkillsRequired Qualifications
  • Bachelor's degree in Biomedical, Mechanical, Manufacturing, Plastics, Polymer Engineering, or a related engineering discipline.
  • 5–10 years of experience in medical device product development, preferably focused on catheter, guidewire, or minimally invasive technologies.
  • Demonstrated experience leading technical development activities within a regulated medical device environment.
  • Strong knowledge of design controls, risk management, verification and validation, and product lifecycle management.
  • Experience developing and optimizing manufacturing processes for medical devices.
  • Excellent technical communication, project leadership, and problem-solving skills.
Preferred Qualifications
  • Master's degree in Engineering or related technical field.
  • Experience within a contract design and manufacturing organization (CDMO) environment.
  • Expertise in catheter or guidewire development technologies.
  • Experience with customer-facing engineering and project leadership.
  • Strong knowledge of FDA, ISO 13485, and MDR requirements.
Core CompetenciesTechnical Competencies
  • Medical Device Product Development
  • Catheter & Guidewire Engineering
  • Design Controls & Product Lifecycle Management
  • Design for Manufacturability (DFM)
  • Design of Experiments (DOE)
  • Verification & Validation (V&V)
  • Risk Management & FMEA
  • Process Development & Optimization
  • Manufacturing Transfer & Scale-Up
  • Prototype Development & Testing
  • Statistical Analysis & Data Interpretation
  • Root Cause Analysis & Problem Solving
  • Technical Documentation
  • FDA & ISO 13485 Compliance
Leadership Competencies
  • Technical Leadership
  • Coaching & Mentoring
  • Stakeholder Management
  • Influencing Without Authority
  • Cross-Functional Collaboration
  • Strategic Thinking
  • Customer Focus
  • Innovation & Continuous Improvement
  • Program Awareness
  • Results Orientation
Why Join Us?
  • Lead cutting-edge medical device development programs that directly impact patient care.
  • Collaborate with industry-leading engineers, clinicians, and global customers.
  • Work on innovative catheter and guidewire technologies from concept through commercialization.
  • Expand your technical leadership and career growth opportunities.
  • Be part of a highly collaborative and mission-driven culture.
  • Receive competitive compensation and comprehensive benefits.

“We don’t just develop devices; we create solutions that help clinicians improve and extend lives.”

Apply