Process Engineering Associate, Co-op/New Grad
at Boston Scientific Corporation
Mississauga, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Dec, 2024 | Not Specified | 29 Sep, 2024 | N/A | Minitab,Engineers,Solidworks,Communication Skills,Six Sigma | No | No |
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Description:
REQUIRED QUALIFICATIONS:
- Actively enrolled in a degree in Engineering or a recent graduate from an Engineering degree
- Strong interest in biomedical technology
- Motivated self-starter with a hands-on approach
- Ability to work independently and with a diverse group of Engineers and Clinicians
- Excellent communication skills, both written and oral
- Strong leadership and problem-solving skills
- Positive attitude and enthusiasm
PREFERRED QUALIFICATIONS:
- Six Sigma or LEAN knowledge
- Experience with SolidWorks and Minitab
- Experience in a highly regulated manufacturing environment
Responsibilities:
ABOUT THE ROLE
The Process Engineering Associate is directly involved in providing product design and manufacturability input during concept and commercialization phases as well as actively participating in continuous improvement initiatives when scaling up existing manufacturing processes.
YOUR RESPONSIBILITIES WILL INCLUDE:
- Support the development and optimization of innovative manufacturing processes and equipment including generating ideas, drafting 3D prototypes in SolidWorks, coordinating testing, and researching and providing input to the team as needed.
- Build and test prototype devices to ensure they meet requirements.
- Assist with the development of validation and test plans by supporting engineers with the execution of process characterization and testing of devices.
- Lead LEAN initiatives to make improvements to the manufacturing process.
- Aid in the development and provision of technical documentation by preparing drawings, writing work instructions, and providing training for new tools and equipment.
- Design test methods or follow standard protocols to ensure the device meets the patients’ needs.
- Monitoring safety practices and ensuring ISO 13485 and FDA compliance while collaborating with cross functional teams to meet product timelines.
- Other duties as required.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Mechanical or Industrial Engineering
Engineering Design / R&D
Mechanical Engineering
Graduate
Engineering
Proficient
1
Mississauga, ON, Canada