Manufacturing Engineer II

Meet Life Sciences; Minnesota; On-site; USD 80,000 - 110,000; Full time

Job summary

Meet Life Sciences is seeking an experienced Manufacturing Engineer II to manage production builds of complex electro-mechanical medical devices across multiple product lines. The role focuses on issue tracking, sustaining BOM and process management, production documentation, and continuous improvement to support safe, high-quality production.

The ideal candidate will have 3–6 years of manufacturing engineering experience in an electronic-based environment, with medical device exposure

Qualifications

• 3–6 years of manufacturing engineering experience in an electronic-based manufacturing environment.
• Medical device manufacturing experience preferred; aerospace manufacturing experience accepted.
• Experience with FDA QSR, ISO 13485, and/or ISO 9001.
• 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.

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 BOMs, assembly and test procedures, part drawings, and ECOs.
• Address quality documentation requirements and work with QA to resolve issues.
• Communicate production status and updates to manufacturing teams.
• Lead continuous improvement initiatives targeting scrap reduction, yield improvement, and efficiency.
• Collaborate cross-functionally with engineering, quality, production, and other teams to meet build plans.

Skills

Manufacturing engineering

Regulated environments

Analytical problem solving

Communication skills

Independent / team work

Tools

SolidWorks

Job description

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.

Required Skills

• 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 SolidWorks.
• 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.