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Manufacturing Engineer II
Job in
Plymouth, Hennepin County, Minnesota, USA
Listed on 2026-09-25
Listing for:
Meet Life Sciences
Full Time
position Listed on 2026-09-25
Job specializations:
-
Manufacturing / Production
Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma, Medical Device Industry
Job Description & How to Apply Below
Seeking an experienced Manufacturing Engineer II to manage production builds of complex electro-mechanical medical devices across multiple product lines. This role will focus on issue tracking and resolution, sustaining BOM and process management, production documentation, continuous improvement, and supporting safe, high-quality production. The ideal candidate will have 3–6 years of manufacturing engineering experience in an electronic-based manufacturing environment, preferably within the medical device industry.
Key Responsibilities- Manage production builds across multiple product lines, including issue tracking, device improvements, and engineering changes.
- Partner with NPI Engineering to transfer new products into sustaining production.
- Create and maintain production documentation, including bills of materials, assembly and test procedures, part drawings, and engineering change orders.
- Address quality documentation requirements and partner with Quality Assurance to resolve product and process issues.
- Communicate production status and updates to manufacturing teams.
- Develop and lead continuous improvement initiatives focused on scrap reduction, yield improvement, labor efficiency, and overall production performance.
- Work directly with customers as needed to support product and manufacturing requirements.
- Maintain awareness of medical device requirements and stay current on new and existing manufacturing processes and industry trends.
- Collaborate cross-functionally with engineering, quality, production, and other internal teams to meet build plans and production goals.
- 3–6 years of manufacturing engineering experience in an electronic-based manufacturing environment.
- Medical device manufacturing experience preferred; aerospace manufacturing experience accepted.
- Experience working in regulated environments, including FDA Quality System Regulations (QSR), ISO 13485, and/or ISO 9001.
- Experience with Solid Works.
- Ability to create, write, and edit technical documentation.
- Strong interpersonal and written/verbal communication skills.
- Strong analytical, troubleshooting, and problem-solving abilities.
- Knowledge of quality improvement tools and continuous improvement techniques.
- Ability to work independently while also collaborating effectively within a team environment.
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