Manufacturing Engineer Intern: Prototyping & Process

Viant Medical; Grand Rapids (MI); On-site; USD 22,000 - 28,000; Part time

Job summary

Viant Medical in Grand Rapids, MI is seeking an Engineering Intern or Co-Op to support production and process improvement under the supervision of the Engineering Supervisor.

You will draft specifications, build prototypes, perform testing, collect data, and contribute to equipment design, while learning Lean and GMP principles in a fast-paced medical device environment.

This role offers hands-on experience with cross-functional teams and exposure to FDA/ISO standards.

Qualifications

• Must be enrolled at an accredited college or university, pursuing a bachelor’s degree in mechanical, industrial, bio-medical or electrical engineering.
• 0-1 years engineering internship or co-op experience.
• Proficiency in Microsoft Office software
• AutoCad and/or Pro Engineer experience

Responsibilities

• Follows GMP and SOPs to meet FDA and ISO standards.
• Develops working relationship with Value Stream team.
• Learns and utilizes Lean concepts in daily work.
• Works independently to complete product sample or prototype builds, perform product testing and gather and analyze test data.
• Drafts component and process specifications and writes/e executes protocols (IQ, OQ, PQ) and change orders (CO).
• Assists ME with drawing tolerance analysis, material analysis, and equipment design support.
• Assists with new product launches and validations.
• Troubleshoots machinery used in manufacturing process and assists Technicians.
• Maintains a project list and reports weekly to Value Stream Manager.
• Develops innovations to improve processes and reduce costs.
• Performs other duties as required

Skills

Microsoft Office

Lean concepts

Education

Bachelor’s degree in engineering (pursuing)

Tools

AutoCad

Pro Engineer

Job description

Viant Medical in Grand Rapids, MI is seeking an Engineering Intern or Co-Op to support production and process improvement under the supervision of the Engineering Supervisor.

You will draft specifications, build prototypes, perform testing, collect data, and contribute to equipment design, while learning Lean and GMP principles in a fast-paced medical device environment.

This role offers hands-on experience with cross-functional teams and exposure to FDA/ISO standards.