Engineering Specialist III

ID# DCCA27469

dinaliC is an international consulting firm specialized in projects for numerous industries. We are dedicated to provide contract and permanent opportunities for skilled professionals in their area or areas of expertise



This position works as a technical expert who can analyze and provide feedback on complex mechanical elements of the device. Candidate shall have strong background in mechanism design concepts, preferably in design and analysis of plastic micro-mechanisms. Performs design and failure analyses, tolerance stack analysis, material research and reliability studies. Provides engineering support for development of IQC methods development, analysis of component FAI and lot release data. 

The successful candidate will demonstrate solid hands-on engineering skills, in addition to use of best practices for design control, GMP, ISO environment. Candidate must be fluent in reading GD&T drawings. 


  • A minimum of a BS Engineering degree in Mechanical
  • Materials Engineering or Biomedical Engineering with a minimum of 6 years relevant engineering experience, or degree with 10 years of relevant engineering experience is required for this role. 
  • Medical device industry experience is preferred. 


  • Strong experience with mechanism design, micro-mechanisms 
  • Highly analytical, attention to detail, employs best documentation practices. 
  • GD&T – fluent reading GD&T drawings, Y14.5-2009 
  • Solidworks proficiency preferred 
  • Expertise in design for plastic injection 
  • Design transfer 

Essential Duties and Responsibilities: include the following. (Other duties may be assigned. )

  • Supports Program DFM effort 
  • Acts as R&D subject-matter-expert for component dimensional characterization, component validation and ongoing formal IQC efforts 
  • Performs design and failure analyses, material research and reliability studies. 
  • May provide guidance and work direction to lower level engineers and technical direction to engineers/designers. 
  • Provide guidance as technical expert in device design, especially in the documentation and specification of device. 
  • Autonomous technical decision making 
  • Compiles and analyzes data, identifies causes, draws conclusions, generates reports 
  • Communicate complex technical material to non-technical audiences 
  • Possibility to supervise overall commercial mold validation, tbd 
  • Fundamental understanding and implementation of Design Control, GMP’s and ISO standards. 
  • 32-40 hours per week, position available immediately.


Position Details:

Medical Device


Start Date: 
End Date: