About the role
DEPARTMENT: Engineering
POSITION OBJECTIVE: The objective of the Engineering Intern is to assist the engineering team throughout the project launch lifecycle by applying knowledge and skills from school to make continuous improvements to processes.
DIRECT REPORTS:
Team Leader – Process Development Engineering
MAJOR DUTIES:
With guidance from Engineering Management:
- Working with all internal departments to document solution assumptions and consolidate the information into proposal framework
- Execution of DOEs (Design Of Experiments) developed by supervising engineer
- Collect and assemble information required to produce price quotations and customer proposals, including technical research, technical communication.
- Facilitate customer design review for gaps to manufacturing requirements for actioning and clarification.
- Document draft process flows, work instructions, process control requirements, and PFMEA’s according to ISO standards.
- Involvement in cross-functional teams and meetings.
- Document and Record Control
WORKING RELATIONSHIPS:
POSITION REQUIREMENTS:
Qualifications
- 3rd or 4th year of university/college engineering co-op program (manufacturing or mechanical) OR a new university/college engineering graduate
- Project management knowledge / experience for priority completion
- ISO 9001 (ISO 13485 a plus).
- Practical knowledge of 2D and 3D drawing softwares.
- Manufacturing environment experience regarding department interaction, equipment, facility, and personnel (Automotive or Medical Devices experience a plus).
- Preference given to mechanical engineering student with production and customer service/business development experience.
Skills and Abilities
- Ideal candidate is enthusiastic, curious, creative, and tenacious with good energy.
- Ability to learn on the fly and work in a high-paced environment.
- Outgoing and customer-facing demeanor
- Ability to problem-solve, work independently and is self-motivated
- Independent, organized, with a high attention to detail
- Proven track record of working well with others in a team environment
- Adapts well to change and shifting priorities
- Excellent Communications skills - internal and external.
REPORTS TO: Engineering Manager
About Sterling Industries
Sterling Industries is a vertically integrated contract manufacturer of medical devices and medical device components with facilities in both the US and Canada. We help companies — from Fortune 100 to mid-size to start-up — scale from launch to full production (whether it be from thousands to millions of units), with consistent and immaculate quality, process and compliance. We offer a repeatable design transfer process, design-for-manufacturing expertise, regulatory compliance and supply chain optimization. Our company mantra is: 100% on time, 100% complete and 100% quality. We manufacture success.
Whether your device requires complicated machined components, intricate injection molded parts, laser cut small diameter stainless steel tubing, laser cut large format metal, robotically welded pieces, integrated electronics, ultrasonic welded parts, and/or low pressure over-molding, our team of engineers, designers and technicians can help make your product a reality. We assemble your device in a Class 7 Clean Room, a White Room or on the Shop Floor as required.
We are ISO 13485:2016 Certified and 21 CFR Part 820 Compliant and are FDA and Health Canada Registered. Let's discuss your project. Contact us by email at sales@sterlingindustries.com or call us toll-free at 1 (888) 669-0246.
About the role
DEPARTMENT: Engineering
POSITION OBJECTIVE: The objective of the Engineering Intern is to assist the engineering team throughout the project launch lifecycle by applying knowledge and skills from school to make continuous improvements to processes.
DIRECT REPORTS:
Team Leader – Process Development Engineering
MAJOR DUTIES:
With guidance from Engineering Management:
- Working with all internal departments to document solution assumptions and consolidate the information into proposal framework
- Execution of DOEs (Design Of Experiments) developed by supervising engineer
- Collect and assemble information required to produce price quotations and customer proposals, including technical research, technical communication.
- Facilitate customer design review for gaps to manufacturing requirements for actioning and clarification.
- Document draft process flows, work instructions, process control requirements, and PFMEA’s according to ISO standards.
- Involvement in cross-functional teams and meetings.
- Document and Record Control
WORKING RELATIONSHIPS:
POSITION REQUIREMENTS:
Qualifications
- 3rd or 4th year of university/college engineering co-op program (manufacturing or mechanical) OR a new university/college engineering graduate
- Project management knowledge / experience for priority completion
- ISO 9001 (ISO 13485 a plus).
- Practical knowledge of 2D and 3D drawing softwares.
- Manufacturing environment experience regarding department interaction, equipment, facility, and personnel (Automotive or Medical Devices experience a plus).
- Preference given to mechanical engineering student with production and customer service/business development experience.
Skills and Abilities
- Ideal candidate is enthusiastic, curious, creative, and tenacious with good energy.
- Ability to learn on the fly and work in a high-paced environment.
- Outgoing and customer-facing demeanor
- Ability to problem-solve, work independently and is self-motivated
- Independent, organized, with a high attention to detail
- Proven track record of working well with others in a team environment
- Adapts well to change and shifting priorities
- Excellent Communications skills - internal and external.
REPORTS TO: Engineering Manager
About Sterling Industries
Sterling Industries is a vertically integrated contract manufacturer of medical devices and medical device components with facilities in both the US and Canada. We help companies — from Fortune 100 to mid-size to start-up — scale from launch to full production (whether it be from thousands to millions of units), with consistent and immaculate quality, process and compliance. We offer a repeatable design transfer process, design-for-manufacturing expertise, regulatory compliance and supply chain optimization. Our company mantra is: 100% on time, 100% complete and 100% quality. We manufacture success.
Whether your device requires complicated machined components, intricate injection molded parts, laser cut small diameter stainless steel tubing, laser cut large format metal, robotically welded pieces, integrated electronics, ultrasonic welded parts, and/or low pressure over-molding, our team of engineers, designers and technicians can help make your product a reality. We assemble your device in a Class 7 Clean Room, a White Room or on the Shop Floor as required.
We are ISO 13485:2016 Certified and 21 CFR Part 820 Compliant and are FDA and Health Canada Registered. Let's discuss your project. Contact us by email at sales@sterlingindustries.com or call us toll-free at 1 (888) 669-0246.