R&D Engineer

Katalyst HealthCares and Life Sciences

$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Mechanical/Biomedical Engineering, Product Design, Materials Engineering, or related discipline.
  • 1-2 years of experience in the Medical Device Industry.
  • Strong analytical and problem-solving skills essential.
  • Working knowledge of CAD software (SolidWorks preferred).
  • Ability to interpret and create technical drawings and engineering documentation.
  • Experience with technical data analysis and presentation.
  • Familiarity with Design Control and Risk Management processes preferred.

Responsibilities

  • Contribute as a core team member on product development projects.
  • Support design activities such as concept development and engineering documentation.
  • Plan and execute studies and tests to support design decisions.
  • Create and maintain engineering documentation including specifications and design records.
  • Utilize CAD software for design activities as needed.
  • Design and coordinate fabrication of tooling and test equipment.
  • Investigate technical issues related to product design and manufacturing processes.
  • Analyze test results to form data-driven conclusions and recommendations.
  • Collaborate with different teams to achieve project objectives.
  • Demonstrate knowledge of Product Development Process and Technology/Product Development systems.

Benefits

  • Collaborative work environment with cross-functional teams.
  • Opportunities for professional growth and development in the medical device field.
  • Involvement in impactful product development projects.
  • Access to advanced technologies and tools in engineering and design.
Full Job Description
Purpose:
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.
  • nalyze 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.'
  • bility 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.

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