Job Description

Combining the spirit of achievement with human and social values has always been a priority at SciCan. Add to this our proven track record of innovation, high quality and dependability, and you'll find a powerful combination that has ensured our growth as a company. We maintain our position as a leader in the health care industry by using a management structure that balances trusting relationships with a creative, dynamic environment.




Being a member of the SciCan family means taking an interest in exploring new paths and using your leadership and strategic planning skills. If you thrive in an exciting, active environment and value quality of life as much as quality of work, we'd like to hear from you. Feel free to send us your resume to hr@scican.com if you're interested in pursuing an opportunity with SciCan in the future.



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Manufacturing Engineer

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Job Summary

This position is responsible to support production activities to ensure consistent high-quality output,productivity improvements and process robustness. This position will also work as a liaison between production and other SciCan departments from product development to the transfer of the product to manufacturing.


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Job Duties & Responsibilities:

Develop, evaluate, and improve manufacturing processes, utilizing knowledge of product design, materials and parts, fabrication processes, tooling and production equipment capabilities, assembly methods, and quality control standards Identify and troubleshoot process, material, or equipment problems to minimize down time. Where possible, apply 6 sigma techniques in the resolution of process, quality, and system deficiencies. Troubleshoot manufacturing issues and drive to closure with related parties. Recommend solutions to design team, if required. Assist production personal in failure analysis and troubleshooting of non-conforming manufactured product to determine the root cause. Design and develop tools, jigs, and fixtures to aid in assembly. Create CAD models and drawings for these tools. Maintain production tools and fixtures. Initiate and lead projects to improve production efficiency, ergonomics and safety of production personals. Prepare reports, charts, and other documentation required for engineering records and projects. Working with Design team at the early stages of new product development ensuring DFM and DFA principals are applied to product design. Develops testing and inspection criteria at various stages of assembly based on the statistical data of parts' reliability and recommendation from the design team. Assist with training of manufacturing employees on new products, tooling, equipment, and process revisions. Identify critical control points and preventive measures. Create and maintain FMEA documents. Using lean concepts and tools, participate in continuous improvement projects to improve production plant and manufacturing processes. Make recommendations and initiate Plant Wide Quality/Process System Improvements including alternative materials, equipment, gauging, systems, error proofing, and methods. Update and document current plant layout. Modify layout as required to support new assembly requirements or new product launch.

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Educational and Experience Requirements:

Bachelor's degree in mechanical, manufacturing or industrial engineering. 5 plus years of related experience in a manufacturing environment preferably with medical products. Working knowledge of manufacturing and quality improvement methods, including Lean Manufacturing concepts. Must be a self-starter, with the ability to work both alone/with minimal supervision and in team environment. Strong analytical and problem-solving skills, with a demonstrated ability to conduct root cause analysis and FMEA (Failure Mode Effect Analysis). Excellent computer and data analysis skills. Candidate must be proficient in Microsoft Office, CAD (Creo preferably), and CMMS systems. Strong communication skills both verbal and written. Certification in Lean Six Sigma (Green Belt, Black Belt) or equivalent will be an asset. * Familiarity with ISO13485 and general product safety requirements such as CSA, UL, TUV will be an asset