Manufacturing Engineer II

Forj Medical; Saint Paul (MN); On-site; USD 80,000 - 95,000; Full time

Benefits offered by this job

Health insurance

Dental benefits

Vision benefits

401(k) plan

Time off

Job summary

Forj Medical in Saint Paul, MN seeks a Manufacturing Engineer II to manage cross-functional production builds of complex electro-mechanical medical devices and to drive process improvements across multiple product lines.

This role will handle issue tracking, BOM and process management, and collaboration with NPI to transfer new products into sustaining production, while ensuring compliant documentation and high-quality outcomes.

Qualifications

• Bachelor's degree in an engineering discipline is required.
• 3–6 years manufacturing engineering experience in electronic-based manufacturing, medical devices preferred.
• Experience with regulated environments (FDA QSRs, ISO 13485, ISO 9001:2000) preferred.

Responsibilities

• Manage production builds of multiple product lines and issues list; collaborate with NP I engineering for transfer to sustaining production.
• Create and maintain production documentation: BOMs, assembly/test procedures, drawings, ECNs.
• Address quality documentation needs; work with QA to resolve quality issues.
• Keep production team informed of status and lead continuous improvement efforts.
• Collaborate with customers as needed and stay current with manufacturing trends.

Skills

Interpersonal communication

Analytical skills

Problem solving

Technical writing

Teamwork

Education

Bachelor's degree in Engineering

Tools

SolidWorks

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 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

EEO Statement

Forj Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Employment Requirement

Must be authorized to work in the United States.

Compensation And Total Rewards Package

The salary range for this position is outlined below under "Job Details" and is dependent upon the individual's skills, experience, qualifications, and applicable employment laws. Beyond base salary, Forj offers a competitive Total Rewards Package. We offer health, dental, vision, 401K plans, and time off programs. You may also be eligible to participate in an annual bonus program which depends on various factors, including, individual and organizational performance.