R&D Engineer

JobDiva, Inc.; Lexington (KY); On-site; USD 65,000 - 95,000; Full time

Job summary

JobDiva, Inc. is seeking an engineer to development and sustain medical device products. You will participate in design activities, prototyping, and analysis to support design decisions and manufacturing improvements.

The role requires strong analytical skills, experience with CAD (SolidWorks preferred), and the ability to interpret engineering drawings and documentation. Collaboration with cross‑functional teams is essential for project success.

Qualifications

• 1-2 years of experience in the Medical Device Industry is preferred.
• Experience supporting product development, sustaining engineering, or manufacturing projects is desirable.
• Proficiency in interpreting and creating technical drawings and engineering documentation.

Responsibilities

• Contribute as a core team member on product development, sustaining engineering, and process improvement projects.
• Support design activities including concept development, prototyping, and engineering documentation.
• Plan and execute engineering studies and testing to support design decisions.
• Create and maintain engineering documentation such as specifications and reports.
• Utilize CAD software to support design of product, fixtures, tooling, and test equipment.

Skills

CAD (SolidWorks)

Analytical thinking

Problem solving

Technical drawings

Documentation

Education

Bachelor's Degree in Mechanical Engineering

Biomedical Engineering or related field

Tools

SolidWorks

Job description

Job Description:

Develops products, materials, processes, and equipment for projects of moderate complexity. Under limited supervision, plans and executes engineering activities to support product development, sustaining engineering, manufacturing, and process improvement initiatives. Compiles, analyses, and reports operational, test, and research data to establish performance standards for new or modified products, processes, and materials.

Roles & Responsibilities:

• Contribute as a core team member on product development, sustaining engineering, and process improvement projects.
• Support product design activities, including concept development, design modifications, prototyping, and engineering documentation.
• Plan and execute engineering studies, experiments, and testing activities to support design and process decisions.
• Create and maintain engineering documentation, including specifications, protocols, reports, drawings, and design records.
• Utilize CAD software (e.g., SolidWorks) to support product, fixture, tooling, and test equipment design activities as required.
• Design, procure, and coordinate fabrication of tooling, fixtures, and test equipment.
• Investigate technical issues related to product design, materials, manufacturing processes, and product performance.
• Analyze test results, identify trends, and formulate data-driven conclusions and recommendations.
• Support engineering change activities and implementation of design or process improvements.
• Collaborate with Manufacturing, Quality, Regulatory, Clinical, and Marketing teams to achieve project objectives.
• 15. Demonstrate knowledge of Product Development Process (PDP) and Technology/Product Development (TPD) systems through delivery of high-quality engineering outputs.

Education & Experience:

• Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, Product Design, Materials Engineering, or a related engineering discipline.
• 1-2 years' experience with in the Medical Device Industry.
• Experience supporting product development, sustaining engineering, or manufacturing projects preferred.
• Strong analytical and problem-solving skills.
• Working knowledge of CAD software (SolidWorks preferred) is desirable.'
• Ability to interpret and create technical drawings and engineering documentation.
• Experience analyzing and presenting technical data.
• Understanding of engineering fundamentals, design principles, and manufacturing processes.
• Experience within a regulated industry, particularly medical devices, is advantageous.
• Familiarity with Design Control, Risk Management, and Engineering Change processes is preferred.
• Proficiency in Microsoft Office applications, including Excel, Word, and PowerPoint.