Role details

Mechanical Project Engineer

New Haven   •  Permanent

Bullet points

  • Medical device company seeking mechanical project engineer
  • 5+ years experience preferred

About Our Client


Job Description

  • Designs, prototypes, tests and develops components, sub-assemblies, systems and full products of up to moderate complexity.
  • Creates test protocols, runs experiments and writes test reports.
  • Completes product documentation of moderate to high complexity.
  • Analyzes moderate to high complexity engineering problems, defines problem, recommends and implements solutions.
  • May lead projects of limited complexity.
  • May lead technicians.
  • Familiarity and experience with Solidworks or Pro/Engineer, GD&T, Finite Element Analysis, free body diagrams, engineering drawings.
  • Design and testing proficiency with rapid prototyping techniques.
  • Design, fabrication and testing proficiency with common manufacturing techniques for high volume, disposable parts - machining, injection molding, stamping, casting, MIM, etc.
  • Experience inventing, innovating and launching products.
  • Proficiency with analysis and problem solving.
  • Proficiency with design of experiments, protocol and model development, testing and documentation.
  • Experience interacting with all functions within a business.
  • Experience in clinical and pre-clinical settings.
  • Ability to utilize common office and web-based software (email, spreadsheets, word processing, presentations) effectively.
  • Ability to present technical materials to non-technical personnel up to President effectively.
  • Knowledgeable of and work within FDA, ISO, CSI and other relevant standards.
  • Ability to use lab testing and fabrication equipment (instron, force gauges, 3d printers, etc.)

The Successful Applicant

  • Bachelor's Degree in Engineering with 5+ years industry experience, Master's degree in engineering management or business with 3+ years industry experience, PhD with 0+ years industry experience.
  • Thorough understanding of medical device manufacturing, especially as it relates to FDA (cGMP) manufacturing requirements.
  • Passing a background check, which may include verification of prior employment, criminal conviction, educational and driving records.

What's on Offer

Competetive base + benefits

Apply for this job

Click the Apply or LinkedIn button below or contact Andrea Albert quoting job reference 1194842
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