Manufacturing Engineer II

Forj Medical • Saint Paul, MN

40d

About The Position

Exceptional People. Hard Problems. Meaningful Careers. Big Impact. Nowhere else can you touch as many life-changing medical technologies. At Forj Medical, we work side by side with more than 100 medical device companies from startups to global giants to bring life-enhancing technologies to market. Working with us means solving hard problems with extraordinary people in a collaborative work environment. Join us. At Forj Medical, the Manufacturing Engineer II will work cross functionally to manage the production build of complex electro-mechanical medical devices. A Manufacturing Engineer II is responsible for the production of multiple product lines. Their responsibilities include: issue tracking and resolution, sustaining BOM and process management, continuous improvement (scrap reduction, yield improvement, labor efficiency improvements), and enabling safe and high quality build plan attainment.

Requirements

• Bachelor’s degree in an engineering discipline.
• 3-6 Yrs experience; (MA 2+ yrs).
• 3 to 6 years manufacturing engineering experience in electronic-based manufacturing environment.
• Medical device preferred, aerospace accepted.
• Experience with regulated environments such as FDA QSR’s, ISO13485 for medical devices and ISO 9001:2000 preferred.
• Experience with SolidWorks
• Ability to write and edit technical documents.
• Strong interpersonal communication.
• Strong analytical skills and problem-solving ability.
• Proficient knowledge of quality improvement tools and techniques.
• Ability to work independently but also function as a team.
• Demonstrated proficiency working with computers and the MS Suite.

Responsibilities

• Manage the production builds of multiple product lines, along with issues list, device improvements and changes.
• Work with NPI engineering to manage the transfer of new products into sustaining production.
• Create and maintain production documentation such as building materials, assembly and test procedures, part drawings, and engineering change orders.
• Address all quality documentation needs for the product line and work with QA to address any quality issues or concerns.
• Keep the production team informed of production status.
• Developed and lead team goals of continuous improvement efforts.
• Work directly with customers as needed.
• Stay current with medical device requirements and maintain technical awareness of new and existing manufacturing processes and trends.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level