What are the responsibilities and job description for the Junior Mechanical Engineer/Developer position at Amico?
Job Summary
Design and development of new products, accessories and spare parts, and engineering support of current products related to manufacturing of suction & oxygen therapy medical devices (flowmeters, suction regulators) and patient room furniture (overbed tables, mother baby equipment, casegoods, carts).
Core Competencies
Job Duties & Responsibilities
The Junior Mechanical Engineer/Developer will work within a team of engineers and developers to perform one or more of the following:
Education & Experience Requirements
Design and development of new products, accessories and spare parts, and engineering support of current products related to manufacturing of suction & oxygen therapy medical devices (flowmeters, suction regulators) and patient room furniture (overbed tables, mother baby equipment, casegoods, carts).
Core Competencies
- Self-motivated and have a hands-on approach
- Strong mechanical aptitude
- Strong oral and written communication skills
- Able to work independently within in a collaborative multi-disciplinary team environment with limited supervision
- Able to effectively manage multiple priorities and meet established deadlines; results-focus
- Sound decision making and judgment capabilities
- Able to adapt to changes quickly in a fast-pace work environment
Job Duties & Responsibilities
The Junior Mechanical Engineer/Developer will work within a team of engineers and developers to perform one or more of the following:
- Be part of a product development team working on support of current products and new product development initiatives
- Design new parts, components, or assemblies for use in new or current products
- Improve design of existing parts to improve manufacturability, reliability or reduce cost where required
- Conduct tolerance stack-up analysis of designs and failure mode and effects analysis (FMEA) of designs and processes as part of risk management where required
- Process engineering changes according to established procedures
- Create and maintain technical/regulatory documentation (design master records & design history files) for new products and design changes
- Develop verification & validation plans and conduct product verification/validation testing
- Participate in design reviews for new parts and products when required
- Build and test prototypes to ensure all essential design requirements are met
- Identify, analyze and correct product or process issues
- Design production jigs and fixtures
- Source and qualify vendors for new part designs and current product parts where required
Education & Experience Requirements
- University Degree in Mechanical or Electro-Mechanical Engineering, P.Eng. status an asset
- 1-3 years of proven working experience in mechanical design, preferably in the area of medical device manufacturing or instrumentation
- Proven experience in designing mechanical components or assemblies from concept to manufacturing
- Proficient in 3D solid modeling CAD (preferably SolidWorks 2019 or above) and detailing.
- Good understanding of Design and Process FMEA an asset
- Exposure to ISO quality systems (ISO 9001 or ISO 13485) and manufacturing environment an asset
- Working knowledge of drafting standards and GD&T an asset
- Working knowledge of plastic injection moulding an asset
- Working knowledge of jig & fixture design an asset
- Basic understanding of electronics an asset
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