Manufacturing Engineer II

Job Description

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.

Job Summary:

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.

Job Duties and 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. 

Qualifications and 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. 

Salary: $80,000 - $95,000