Mechanical Engineers

Intuvie

$104K — $108K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's Degree in Mechanical Engineering, Materials Science & Engineering, or Biomedical Engineering
  • Proficiency in Advanced Mechanical Design and 3D CAD Modeling
  • Experience with Tolerance Analysis and Mechanical Stack-up Evaluation
  • Knowledge of QMS and Manufacturing Integration
  • Familiarity with FDA 510 (K) regulatory compliance processes

Responsibilities

  • Develop and implement designs for medical devices
  • Analyze and interpret mechanical assemblies using AutoCAD and SolidWorks
  • Coordinate product release according to the NPI process
  • Evaluate materials under mechanical stress and environmental exposure
  • Optimize product design and change controls during the engineering process
  • Create standard operating procedures (SOP) and document design changes
  • Provide technical solutions for manufacturing transfer and ramp-up

Benefits

  • Opportunity to work with cutting-edge medical device technology
  • Involvement in all phases of product lifecycle from design to market
  • Contribute to compliance with FDA regulations
  • Collaborative work environment focused on innovative engineering solutions
  • Hands-on experience with advanced testing and manufacturing methodologies
Full Job Description
Develop and implement mechanical engineering design for medical devices using knowledge of Advanced Mechanical Design, Python, MATLAB; Design, analyze, and interpret complex mechanical assemblies using AutoCAD, SolidWorks 3D/2D modeling, GD&T (Geometric dimensioning and tolerancing) practices; Coordinate product releases in compliance of NPI process, and complete design verification and validation; Evaluate material behavior under mechanical stress, environment exposure, and long-term usage conditions using mechanical test equipment, Formlab 3D Printer, IQ/OQ/PQ, d-FMEA, u-FMEA; Review and optimize product design and change controls in the manufacturing and engineering process using QMS, Manufacturing Integration; Ensure proper alignment between pump drive components and administration set using Tolerance Analysis and Mechanical Stack-up Evaluation; Create SOP and document technical design and process changes of medical devices; Coordinate manufacturing at client sites and implement DFM (Design for Manufacturing) concepts, to ensure successful product release; Provide technical solutions and guidance for the manufacturing transfer and ramp up process using Manufacturing system integration concepts; Diagnose and troubleshoot medical devices using principles of Electro-mechanical system; Ensure FDA 510 (K) regulatory compliance of premarket notification submissions for Class II medical devices.

Must have a Master's Degree in Mechanical Engineering, Materials Science & Engineering, or Biomedical Engineering plus skills and knowledge in Advanced Mechanical Design, 3D CAD Modeling, Tolerance Analysis, Mechanical Stack-up Evaluation, SOP, QMS, Manufacturing Integration, 510 (K) Regulatory Compliance.

Job location: Natick, MA. $104,042~$108k per year. Submit résumé referencing job code BIY002 to HR, Zyno Medical, LLC, 177 Pine Street, Natick, MA 01760.

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