Senior Medical Device Manufacturing Engineer: NPI & Scale
Job in
Minneapolis, Hennepin County, Minnesota, 55400, USA
Listed on 2026-05-28
Listing for:
Energy Jobline ZR
Full Time
position Listed on 2026-05-28
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering, Process Engineer, Medical Device Industry -
Manufacturing / Production
Manufacturing Engineer, Quality Engineering, Medical Device Industry
Job Description & How to Apply Below
Job Description
Job Title Sr. Manufacturing Engineer
Location:
Plymouth, MN, 55442
Duration : 6 months with Possible Extension
No Benefits Provided
Seeking a motivated and results-driven Senior Manufacturing Engineer to support New Product Introduction (NPI) and manufacturing operations for medical device products. This role will focus on yield improvement, process optimization, product transfer, and manufacturing scale-up in a fast-paced production environment.
Key Responsibilities
- Lead yield and productivity improvement projects across manufacturing processes.
- Support new product introduction (NPI), pilot builds, and transfer to production.
- Troubleshoot manufacturing issues using Root Cause Analysis, DMAIC, and other problem-solving tools.
- Analyze manufacturing data to improve quality, efficiency, and throughput.
- Coordinate tooling, equipment, and process development activities.
- Collaborate with Operations, Quality, R&D, Supply Chain, and Regulatory teams.
- Ensure compliance with FDA, ISO 13485, GMP, and quality system requirements.
- Mentor junior engineers and support continuous improvement initiatives.
Required Qualifications
- Bachelor’s degree in Mechanical, Biomedical, Chemical, or related Engineering field from a US institution.
- 3–5+ years of experience in medical device manufacturing or process engineering.
- Experience with NPI, process development, or manufacturing support.
- Strong analytical, troubleshooting, and project management skills.
- Ability to provide examples of process improvements, yield improvements, or productivity enhancements implemented.
- Strong communication and teamwork skills.
Qualifications
- Experience in catheter or medical device manufacturing.
- Knowledge of assembly, bonding, soldering, reflow, or packaging processes.
- Experience working in FDA and ISO-regulated environments.
Additional Details
- Location:
Plymouth - Schedule:
8:30 AM – 5:30 PM - Travel:
Up to 25% including international travel.
Position Requirements
10+ Years
work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×