Sr. Engineer, R&D (Biomaterials)

Axogen, Inc.; Tampa (FL); On-site; USD 92,000 - 115,000; Full time

Benefits offered by this job

Annual bonus

Health, Dental, Vision

Matching 401K

Paid time off

Floating holidays

Employee Stock Purchase Plan

Tuition Reimbursement

Parental Leave

Disability Insurance

Job summary

Axogen, Inc. is seeking a Sr. Engineer, Research & Development to lead the development of innovative products for peripheral nerve injury treatment from concept to commercialization.

This role collaborates with Quality Assurance, Regulatory Affairs, Operations, Marketing, and Medical Affairs to ensure alignment and effective project execution. The Senior Engineer must demonstrate strong technical communication skills and apply biomaterials expertise to solve design challenges, manage multiple

Qualifications

• Bachelor's degree required in a relevant engineering field.
• Minimum of 5 years in the medical device or pharmaceutical industry.
• Product development experience required.
• Experience applying biomaterial composition, structure, and chemistry to design challenges.
• Experience with clinical surgical environments preferred.
• FDA-regulated industry with ISO and QSR exposure preferred.
• Understanding of design controls, risk management, and verification/validation in a medical device environment.
• Ability to communicate technical information clearly to diverse audiences.

Responsibilities

• Lead development of new products to treat peripheral nerve injuries from concept through commercialization.
• Serve as the technical lead for product development projects of moderate complexity.
• Collaborate with Quality, Regulatory, Operations, Marketing, Medical Affairs, and other stakeholders.
• Engage with external customers and internal stakeholders to translate needs into requirements.
• Generate, prototype, and evaluate concepts and designs.
• Optimize designs through testing, experimentation, analysis, and evaluation.
• Execute verification and validation activities per Design Controls and regulatory standards.
• Participate in risk management activities including hazard identification and mitigation.
• Communicate technical information clearly to internal and external audiences.
• Ensure activities comply with FDA/ISO requirements and maintain documentation.
• Contribute to Axogen's intellectual property portfolio.
• Maintain detailed documentation throughout all development phases.
• Stay current with developments in relevant technical areas.
• Provide guidance and mentorship to less-experienced team members.

Skills

Biomaterials knowledge

Technical communication

Problem solving

Cross-functional collaboration

Education

Bachelor's degree in Biomedical/Mechanical/Chemical/Materials science or related field

Job description

Axogen is committed to building and maintaining a strong and gratifying company culture that fosters professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process. Most benefits are effective on day one! Axogen is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status.

Why you'll love working at Axogen:

• Friendly, open, and fun team culture that values unique perspectives
• Company-wide dedication to profoundly impacting patients' lives
• Comprehensive, high-quality benefits package effective on date of hire
• Educational assistance available for all employees
• Matching 401(k) retirement plan
• Paid holidays, including floating holidays, to be used at your discretion
• Employee Stock Purchase Plan
• Referral incentive program

Axogen Mission and Business Purpose

Our business purpose is to restore health and improve quality of life by making restoration of peripheral nerve function an expected standard of care. We aim to lead the markets we serve by always requiring the solutions we offer patients and caregivers provide an improved benefit-to-risk profile as compared to existing standards of care. To ensure we deliver improved benefit-to-risk solutions, we will guide and expect the market and design requirement specifications underlying our engineering, business development, and clinical research activities, objectively target advancements in standards of care.

Job Summary of the Sr. Engineer, R&D

The Sr. Engineer, Research & Development, is an experienced product development professional responsible for leading the development of innovative products to treat peripheral nerve injuries from concept through commercialization. This role collaborates closely with cross-functional teams including Quality Assurance, Regulatory Affairs, Operations, Marketing, and Medical Affairs to ensure alignment and effective project execution. The Senior Engineer must demonstrate strong technical communication skills and effectively adapt communication to a variety of internal and external audiences. For this position, experience in biomaterials development is strongly preferred. The ideal candidate will leverage expertise in biomaterials composition, structure, and chemistry to solve product design challenges, optimize material formulations, and drive desired performance in biological environments. This role requires designing and executing studies, analyzing data, drawing conclusions, and providing technical recommendations to support the successful development of new products and technologies. The position demands a proactive approach to problem solving, an understanding of medical device design controls and regulatory requirements, and the ability to manage multiple projects and priorities while maintaining a high level of attention to detail. The Senior Engineer is expected to independently lead product development projects of moderate complexity and contribute technical expertise to larger and more complex development programs.

Requirements of the Sr. Engineer, R&D

• Bachelor's degree required in Biomedical Engineering, Mechanical Engineering, Chemical Engineering, Materials Science and Engineering, or a related field.
• Minimum of 5 years of experience in the medical device or pharmaceutical industry.
• Product development experience required.
• Demonstrated ability to apply an understanding of biomaterial composition, structure, and chemistry to solve product design challenges and drive desired performance in biological environments.
• Experience with clinical surgical environments preferred.
• Experience working in an FDA-regulated industry with ISO and Quality System Regulation requirements preferred.
• Demonstrated understanding of product development processes, design controls, risk management principles, and verification and validation methodologies within a regulated medical device environment.
• Demonstrated ability to communicate technical information clearly and effectively to diverse audiences, including the preparation and delivery of technical presentations.

Responsibilities of the Sr. Engineer, R&D

• Applies expertise in biomaterials composition, structure, and chemistry to solve product design challenges and optimize product performance in biological environments Leads the development of new products to treat peripheral nerve injuries from concept through commercialization, including medical devices, tissues, biologics, and combination products.
• Serves as the technical lead for product development projects of moderate complexity and contributes technical expertise to larger or more complex development programs.
• Collaborates cross-functionally with Quality, Regulatory, Operations, Marketing, Medical Affairs, and other key stakeholders to support successful product development and project execution.
• Engages with external customers and internal stakeholders to understand user needs and translate those needs into product and design requirements.
• Generates, prototypes, and evaluates concepts and designs.
• Optimizes designs through testing, experimentation, analysis, and evaluation.
• Executes product development activities in accordance with Design Control requirements, applicable quality system procedures, and relevant regulatory standards.
• Plans and executes verification and validation activities to ensure products meet user needs, design requirements, and intended uses.
• Participates in and may lead risk management activities including hazard identification, risk analysis, implementation of risk controls, and evaluation of residual risk.
• Applies sound technical expertise and engineering judgment to design and conduct studies, analyze quantitative data, draw conclusions, and provide technical recommendations.
• Effectively communicates technical information in a clear and accessible manner to both internal and external audiences.
• Ensures assigned activities are performed in compliance with relevant regulatory and industry standards (e.g., FDA, ISO).
• Contributes to Axogen's intellectual property portfolio through invention disclosures, technical contributions, and related activities.
• Maintains appropriate detailed documentation throughout all phases of Research and Development.
• Investigates and evaluates new and existing technologies and remains current with developments in relevant technical areas.
• Provides guidance, training, and mentorship to less-experienced team members.

Location 111 West Oak Ave., Tampa, FL 33602 #LI-AC1

Benefits/Compensation

• This position is eligible for an annual bonus.
• Benefits offered for this position include Health, Dental, Vision, Matching 401K, Paid Time Off, 9 Paid Holidays + 3 Floating Holidays, Dependent Care Flexible Spending Accounts, Medical Flexible Spending Accounts, Tuition Reimbursement, Paid Parental Leave, Paid Caregiver Leave, Basic Life Insurance, Supplemental Life Insurance, Employee Stock Purchase Plan, and Disability Insurance, as described in more detail in summary plan descriptions.

Salary Range$92,293 - $115,367 USD

Axogen follows healthcare system guidelines with respect to credentialing, vaccinations and other employment/compliance related requirements, as well as CDC guidance. Axogen reserves the right to amend its policies from time to time in its sole discretion. As AI is becoming a common tool throughout the application process, we want to be clear about its appropriate use at Axogen. Using AI to support resume writing, research or interview preparation is perfectly acceptable, provided the content is accurate and genuinely represents your qualifications and skills. For other key parts of your interview process, however, it is important that the ideas, communication, and work you share reflect your own voice, experiences, and thinking. We ask that you participate in our live interviews and complete any assessments without AI assistance unless instructions explicitly indicate otherwise or a specific exception is discussed and approved in advance. This approach ensures fairness, celebrates your individuality, and allows your authentic perspective to shine. Behaviors that do not align with these guidelines may result in disqualification from the hiring process or termination of employment if later discovered. We appreciate your understanding and look forward to learning about the unique contributions only you can bring to Axogen.