R&D Engineer

Katalyst HealthCares and Life Sciences

$90K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Mechanical, Biomedical, Electrical, Manufacturing, Industrial Engineering, or related field.
  • 3-8+ years in R&D, Product Development, or Design Engineering.
  • Experience in product design, prototype development, and engineering documentation.
  • Proficiency in CAD software (SolidWorks, Creo, CATIA, AutoCAD, Siemens NX).
  • Strong understanding of engineering principles, materials, and manufacturing processes.
  • Experience with Design Verification & Validation (V&V).
  • Strong analytical, problem-solving, and troubleshooting skills.

Responsibilities

  • Design and enhance new products, components, and manufacturing processes.
  • Support product development from concept to commercialization.
  • Produce engineering drawings and technical documentation.
  • Develop prototypes and conduct feasibility studies for performance evaluation.
  • Plan and execute design verification and validation testing.
  • Conduct root cause analysis and correct product/process issues.
  • Collaborate with cross-functional teams for design transfer and production readiness.

Benefits

  • Collaborative work environment with cross-functional teams.
  • Opportunities for continuous product improvement and professional growth.
  • Engagement in innovative projects with potential impact.
  • Exposure to various engineering disciplines and industries.
Full Job Description
Job Description:
We are seeking an innovative and detail-oriented R&D Engineer to support the research, design, development, and validation of new products and technologies. The ideal candidate will collaborate with cross-functional teams to transform concepts into commercially viable products while ensuring compliance with quality, regulatory, and customer requirements. This role involves product design, prototyping, testing, risk analysis, design verification and validation, and continuous product improvement throughout the development lifecycle.
Responsibilities:
  • Design, develop, and improve new products, components, and manufacturing processes.
  • Support all phases of product development, from concept through commercialization.
  • Create engineering drawings, specifications, and technical documentation.
  • Develop prototypes and conduct feasibility studies to evaluate product performance.
  • Plan and execute design verification and validation (V&V) testing.
  • Perform root cause analysis and implement corrective actions for product and process issues.
  • Conduct Design Failure Mode and Effects Analysis (DFMEA), Process FMEA (PFMEA), and risk assessments.
  • Collaborate with Manufacturing, Quality, Regulatory, Supply Chain, and Operations teams to support design transfer and production readiness.
  • Support process validation activities, including IQ/OQ/PQ, as required.
  • nalyze test data and prepare engineering reports and technical presentations.
  • Ensure compliance with applicable industry standards, regulatory requirements, and company quality systems.
  • Drive continuous improvement initiatives to enhance product quality, reliability, and manufacturability.
  • Participate in design reviews, technical risk assessments, and engineering change activities.

Requirements:
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Manufacturing Engineering, Industrial Engineering, or a related engineering discipline.
  • 3-8+ years of experience in Research & Development, Product Development, or Design Engineering.
  • Experience with product design, prototype development, testing, and engineering documentation.
  • Proficiency in CAD software such as SolidWorks, Creo, CATIA, AutoCAD, or Siemens NX.
  • Strong understanding of engineering principles, materials, and manufacturing processes.
  • Experience with Design Verification & Validation (V&V).
  • Knowledge of Design Controls, Risk Management, and Design Reviews.
  • Strong analytical, problem-solving, and troubleshooting skills.
  • Excellent written and verbal communication skills.
  • bility to work effectively in a cross-functional team environment.

Preferred Qualifications:
  • Experience in Medical Devices, Biotechnology, Life Sciences, Aerospace, Automotive, Consumer Products, or Advanced Manufacturing.
  • Knowledge of ISO 13485, FDA 21 CFR Part 820/QMSR, ISO 14971, or ISO 9001 (depending on industry).
  • Experience with statistical analysis tools such as Minitab or JMP.
  • Familiarity with DOE (Design of Experiments), GD&T, tolerance analysis, and DFM/DFA principles.
  • Experience supporting New Product Introduction (NPI) and design transfer activities.

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