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Contract Biomedical Product Development Engineer Jobs in Florida

KLS Martin

R&D Engineer I (34655)

Jacksonville, FL · On-site

... and product management. Educational and Experience Requirements * BS in Engineering (Mechanical, Bioengineering, Biomedical) or comparable technical/medical field * Prior experience with 3D CAD ...

KLS Martin

R&D Engineer II (34656)

Jacksonville, FL · On-site

Our product portfolio includes titanium and resorbable implants for reconstruction, innovative ... Educational and Experience Requirements * BS in Engineering (Mechanical, Bioengineering, Biomedical ...

amphenol

R&D Engineer

Saint Augustine, FL

As a Research and Development (R&D) Engineer, you will play a key role in driving innovation, new product development, and process improvements that support customer requirements and business ...

amphenol

R&D Engineer

Saint Augustine, FL · On-site

As a Research and Development (R&D) Engineer, you will play a key role in driving innovation, new product development, and process improvements that support customer requirements and business ...

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Contract Biomedical Product Development Engineer information

What does a contract biomedical product development engineer do?

A Contract Biomedical Product Development Engineer is a specialized professional who works on a temporary or project basis to design, develop, and improve medical devices and products. They collaborate with multidisciplinary teams to ensure products meet regulatory standards, are safe for patients, and function as intended. Their responsibilities often include prototyping, testing, and documenting development processes, as well as troubleshooting and refining designs based on feedback and test results. This role is vital for bringing innovative healthcare solutions to market efficiently and effectively.

How does a contract biomedical product development engineer typically interact with cross-functional teams during a project?

As a Contract Biomedical Product Development Engineer, you will regularly collaborate with cross-functional teams, including regulatory affairs, quality assurance, manufacturing, and clinical teams. You may participate in design reviews, coordinate testing protocols, and ensure that the product meets both engineering and compliance standards. Effective communication and documentation are essential, as you often serve as a liaison between technical and non-technical stakeholders. These collaborations help streamline the development process and ensure that project milestones are met on time.

What are the key skills and qualifications needed to thrive as a contract biomedical product development engineer, and why are they important?

To thrive as a Contract Biomedical Product Development Engineer, you need a strong background in biomedical engineering principles, product design, and regulatory compliance, usually supported by a relevant engineering degree. Familiarity with CAD software, prototyping tools, and standards such as ISO 13485 or FDA regulations is typically required. Exceptional problem-solving, project management, and collaboration skills help you drive projects forward and adapt quickly in dynamic environments. Mastery of these skills ensures innovative, safe, and compliant medical products are developed efficiently to meet client and regulatory expectations.

What is the difference between Contract Biomedical Product Development Engineer vs Contract Biomedical Research Scientist?

AspectContract Biomedical Product Development EngineerContract Biomedical Research Scientist
CredentialsBachelor's or Master's in Biomedical Engineering, related fieldBachelor's or Master's in Biology, Biomedical Science, or related field
Work EnvironmentDesign, develop, and test medical devices and products in R&D labs or manufacturing settingsConduct experiments, analyze biological data, and study disease mechanisms in research labs
Employer & Industry UsageMedical device companies, biotech firms, healthcare product developersResearch institutions, biotech companies, pharmaceutical firms

The Contract Biomedical Product Development Engineer focuses on designing and developing medical devices and products, working closely with engineering teams. In contrast, the Contract Biomedical Research Scientist conducts biological research to understand disease processes or test biological hypotheses. Both roles require scientific credentials but differ in their primary focus and work environment.

What are the most commonly searched types of Biomedical Product Development Engineer jobs in Florida?

The most popular types of Biomedical Product Development Engineer jobs in Florida are:

What cities in Florida are hiring for Contract Biomedical Product Development Engineer jobs?

Cities in Florida with the most Contract Biomedical Product Development Engineer job openings:

Contract Biomedical Product Development Engineer jobs near you
Infographic showing various Contract Biomedical Product Development Engineer job openings in Florida as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution.

Manufacturing Engineer (All Levels), New Product Development

Exactech

Gainesville, FL • On-site

Full-time

Re-posted 27 days ago

Exactech rating

8.0

Company rating: 8.0 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

The New Product Development (NPD) Engineer is responsible for representing Manufacturing Engineering throughout the product development lifecycle. This role serves as the voice of manufacturing on crossfunctional project teams and ensures that product designs are manufacturable, scalable, compliant, and released on schedule.  
The NPD Engineer partners closely with R&D, Quality, Supply Chain, and Operations to drive design for manufacturability (DFM), ensure timely completion of manufacturing deliverables, and support successful transfer of new products into production in compliance with applicable regulatory and quality system requirements.
  • Act as the manufacturing engineering representative on new product development and sustaining project teams. 
  • Lead and influence Design for Manufacturability (DFM) and Design for Assembly (DFA) activities throughout the design lifecycle. 
  • Review and provide formal manufacturing input on product designs, drawings, specifications, and change orders. 
  • Ensure all manufacturing-related deliverables are completed accurately, on time, and in alignment with project timelines. 
  • Define and document manufacturing processes, equipment requirements, tooling, fixtures, and work instructions for new products. 
  • Support and/or lead process validation activities (IQ/OQ/PQ) in collaboration with Quality Engineering. 
  • Partner with Quality to ensure compliance with FDA, ISO, and internal Quality System requirements during product development and transfer. 
  • Identify manufacturing risks early and drive mitigation plans to support robust product launches. 
  • Support pilot builds, first article builds, and production ramp up activities. 
  • Collaborate with Supply Chain to support supplier selection, supplier readiness, and manufacturability of purchased components. 
  • Provide technical support during design reviews, risk assessments (e.g., PFMEA), and change management activities. 
  • Contribute to continuous improvement initiatives related to manufacturing efficiency, quality, and cost. 
  • Maintain accurate documentation in accordance with document control and change management procedures.
Education:
  • Bachelor's degree in Engineering (Manufacturing, Mechanical, Biomedical, Industrial, or related field) required
 Experience:
  • Minimum 1-5 years experience in manufacturing engineering within a regulated environment (medical device, aerospace, automotive, or similar). 
  • Experience supporting new product development and product transfer to manufacturing. 
  • Demonstrated experience applying DFM/DFA principles to product designs.
Functional/Technical Knowledge, Skills and Abilities Required:
  • Strong understanding of manufacturing processes, tooling, fixtures, and production equipment. 
  • Working knowledge of quality systems, validation requirements, and regulatory standards (e.g., FDA, ISO). 
  • Ability to interpret engineering drawings, specifications, and GD&T. 
  • Strong cross functional collaboration and communication skills. 
  • Proven ability to manage multiple deliverables and meet project deadlines. 
  • Experience with risk management tools such as PFMEA preferred. 
  • Proficiency with standard engineering and documentation tools (e.g., CAD viewers, ERP/MRP, document control systems). 

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