Medical Components, Inc. logo
Medical Components, Inc.
Posted 76 days agoVerified live 17h ago

Materials Engineer

Brief overview

Remote
UndergradOr in progress
3+ yrsMinimum
Material characterizationMaterial selectionISO 10993ISO 14971EU MDRFDA GuidanceMedical device manufacturingCAD software - SolidWorksInjection moldingExtrusionGD&TEngineering drawingsValidation testing methodsStatistical analysisFEAMold flow analysisMicrosoft Office

About the company

Medical Components, Inc. logo
Medical Components, Inc.medcompnet.com

Medical Components is a medical devices company that offers vascular access devices.

Job description

Summary

Medical Components, Inc. is seeking a Materials Engineer to provide technical expertise in material selection and qualification for the design and development of disposable medical devices. The role involves collaboration with cross-functional engineering teams and ensuring adherence to Design Control standards, quality systems, and regulatory requirements.

Responsibilities

  • Lead material selection and qualification processes for product design and development
  • Evaluate material changes and define/execute required validation and testing
  • Review product designs for material manufacturability, performance, and cost efficiency
  • Ensure proper review and release of materials, drawings, and documentation
  • Assess material properties and compatibility for intended product use
  • Collaborate with suppliers to define material processing and support production needs
  • Collaborate with Biocompatibility, Manufacturing, Research & Development (R&D), and New Product Development (NPD) teams to support material science, chemical characterization, and product safety activities for FDA, EU MDR, and global regulatory submissions, technical documentation, and regulatory responses
  • Evaluate material composition, additives, impurities, processing aids, degradation products, and residual chemicals
  • Assess material, supplier, formulation, manufacturing, sterilization, and packaging changes, determine requires testing, validation, risk assessment, and regulatory documentation for proposed changes
  • Prepare responses to FDA, notified body, and other regulatory deficiencies related to materials and biocompatibility
  • Interpret and review complex chemical data sets from outside analytical and biological laboratories and compare results to supplier documentation
  • Evaluate scientific evidence and develop defensible conclusions using a weight-of-evidence approach
  • Maintain material and material property databases
  • Support manufacturing operations and resolve production issues
  • Travel to other facilities as needed (5–15%)

Skills

  • Bachelor's degree in Materials Science, Polymer Science, Chemistry or related technical field
  • 3–5 years of experience in manufacturing or medical device industry
  • Strong experience in material characterization and selection in accordance with ISO 14971, ISO 10993 Series of Standards, EU MDR, and FDA Guidance
  • Experience in engineering design, validation, and product testing environments
  • Knowledge of ISO 10993, ISO 14971 is required
  • Familiarity with FDA, GMP, GLP, and EU MDR regulations
  • Knowledge of injection molding, extrusion, and secondary operations
  • Understanding of GD&T and engineering drawings
  • Experience with validation testing methods and statistical analysis
  • Strong problem-solving and analytical abilities
  • Excellent written and verbal communication skills
  • Ability to lead projects and mentor team members
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Project, Outlook)
  • Ability to sit, stand, walk, and use hands regularly
  • Occasional lifting up to 25 lbs
  • Ability to work in manufacturing, lab, and prototype environments
  • Vision abilities including close and distance vision, color vision, and depth perception
  • Combination of office, manufacturing floor, engineering lab, and prototype shop environments
  • Exposure to mechanical equipment and moderate noise levels
  • Must have or be able to obtain a valid passport
  • Experience with CAD software (SolidWorks preferred)
  • Familiarity with FEA and mold flow analysis

Qualifications

Must Haves

  • Bachelor's degree in Materials Science, Polymer Science, Chemistry or related technical field
  • 3–5 years of experience in manufacturing or medical device industry
  • Strong experience in material characterization and selection in accordance with ISO 14971, ISO 10993 Series of Standards, EU MDR, and FDA Guidance
  • Experience in engineering design, validation, and product testing environments
  • Knowledge of ISO 10993, ISO 14971 is required
  • Familiarity with FDA, GMP, GLP, and EU MDR regulations
  • Knowledge of injection molding, extrusion, and secondary operations
  • Understanding of GD&T and engineering drawings
  • Experience with validation testing methods and statistical analysis
  • Strong problem-solving and analytical abilities
  • Excellent written and verbal communication skills
  • Ability to lead projects and mentor team members
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Project, Outlook)
  • Ability to sit, stand, walk, and use hands regularly
  • Occasional lifting up to 25 lbs
  • Ability to work in manufacturing, lab, and prototype environments
  • Vision abilities including close and distance vision, color vision, and depth perception
  • Combination of office, manufacturing floor, engineering lab, and prototype shop environments
  • Exposure to mechanical equipment and moderate noise levels
  • Must have or be able to obtain a valid passport

Nice to Haves

  • Experience with CAD software (SolidWorks preferred)
  • Familiarity with FEA and mold flow analysis

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