Intermediate Mechanical Engineer – R&D (Medical Devices) at Ball Service Group Inc
Kitchener, ON, Canada -
Full Time


Start Date

Immediate

Expiry Date

06 Dec, 25

Salary

32.0

Posted On

07 Sep, 25

Experience

6 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Electrical Equipment, Mechanical Testing, Iso, Communication Skills, Materials, Specifications, Solidworks, Life Sciences, Manufacturing Processes, Regulatory Requirements, Robotics, Medical Devices, Design Engineering, 3D Printing, Precision Machining, Stairs

Industry

Mechanical or Industrial Engineering

Description

At Ball Service Group, we pride ourselves on our proven track record in the design and manufacturing of custom large-scale assemblies. In recent years, we have expanded our expertise to include high-accuracy, electronically controlled small assemblies - delivering micron-level precision solutions tailored for OEMs.
We are seeking a talented and motivated Intermediate Mechanical Engineer to join our Research & Development team focused on pathology and diagnostic medical devices. The successful candidate will play a key role in designing, developing, and testing innovative mechanical solutions that support next-generation pathology instrumentation devices. This position involves working in a multidisciplinary environment with scientists, electrical engineers, software developers, mechanical engineers, and clinical experts to bring advanced diagnostic tools from concept through commercialization.

QUALIFICATIONS:

  • Bachelor’s degree in mechanical engineering or related field
  • 3–6 years of experience in mechanical design engineering, preferably in the medical device, life sciences, or diagnostics industry
  • Proficiency in 3D CAD (SolidWorks) and PDM systems
  • Strong foundation in mechanical design, materials, precision machining, and manufacturing processes
  • Knowledge of CNC machining, welding principles, and 3D printing
  • Experience with motion systems, and optics integration is highly desirable
  • Familiarity with regulatory requirements for medical devices (ISO 13485, FDA 21 CFR Part 11/820)
  • Hands-on experience with prototyping, mechanical testing, and lab instrumentation
  • Creative thinker and capable of leveraging AI tools to improve and automate design and manufacturing processes
  • Excellent problem-solving, organizational, and communication skills
  • Ability to thrive in a fast-paced R&D environment with cross-disciplinary collaboration
  • Experience with automated systems, robotics, or laboratory instrumentation

PHYSICAL AND MENTAL REQUIREMENTS:

  • Ability to read and interpret technical drawings and specifications.
  • Ability to operate basic mechanical and electrical equipment with minimal training.
  • Ability to walk or stand for extended periods on concrete surfaces.
  • Ability to climb stairs and ladders as required.
  • Strong communication skills to effectively collaborate with team members.
  • Ability to conduct normal ordering and basic scheduling calculations.
Responsibilities

OPERATIONAL RESPONSIBILITIES:

  • Lead the design and development of mechanical components and assemblies for medical devices, ensuring precision, reliability, and manufacturability.
  • Develop detailed 3D CAD models, assemblies, and technical drawings in SolidWorks, maintaining compliance with engineering specifications and regulatory standards.
  • Evaluate engineering requirements, including materials, dimensions, machining techniques, finishes, and process parameters, to ensure design feasibility and performance.
  • Perform engineering analysis such as tolerance stack-ups, FEA, thermal, and motion/kinematic studies to validate designs.
  • Collaborate with cross-functional teams to integrate mechanical systems with electronics, optics, motion control, and automation.
  • Generate and maintain bills of materials (BOMs), documentation, and engineering records to support development and production.
  • Drive prototyping efforts, including hands-on assembly, testing, and iterative design refinement.
  • Engage with suppliers to source precision components, assess manufacturability, and ensure quality for prototypes and production.
  • Facilitate the transfer of designs from R&D to manufacturing, incorporating design-for-manufacturing (DFM) and design-for-assembly (DFA) principles.
  • Plan and coordinate projects, including timelines, procurement, in-house labor, and vendor collaboration, to ensure on-time, on-budget delivery.
  • Support product development initiatives aligned with company strategy, including value engineering and process improvement to optimize cost, quality, and efficiency.
  • Oversee quality assurance throughout all project phases, from work-in-progress inspections to final product verification.
  • Provide technical guidance and support to shop personnel during assembly and testing.
  • Maintain accurate project documentation and contribute to continuous improvement initiatives.

HEALTH AND SAFETY RESPONSIBILITIES:

  • Ensure safe and healthy conditions exist for all employees.
  • Comply with the Occupational Health and Safety Act (OHSA), Regulation 851 – Industrial Establishments, and BSG’s Health & Safety policies.
  • Work in accordance with the Quality Management System ISO 9001:2015.
  • Ensure safe working conditions by using required protective equipment and following safe operating procedures.
  • Take every reasonable precaution to protect oneself and others and promptly report unsafe conditions or hazards.
Loading...