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