Website restor3d



restor3d enables surgeons to improve the reconstruction and repair of the human body through 3D printed implants with enhanced anatomical fit and superior integrative properties. We leverage expertise and experience in 3D printing of key biomedical materials spanning a wide range of properties, seeking to improve medical device solutions.


The Head of Manufacturing Engineering will function as a subject matter expert and will be responsible for the development of manufacturing strategy in support of new products at restor3d. The ideal candidate will have a proven track record of excellence and passion for development of new processes and products within the medical device industry. This individual must be a strong leader with experience fostering an environment for personal development of teams they manage.


Principal responsibilities for the position include the following. Other duties may be assigned as necessary.

-Define and implement manufacturing strategy in support of new product development.

-Lead Manufacturing Engineers in process improvements and new product introduction.

-Collaborate with senior management in the development, planning, and execution ofannual business plans, budgets, capital plans and performance goals and objectives foreach department.

-Supports root cause investigations and manufacturing process improvements

-Ensure quality goals are met and continuous improvement of manufacturingperformance.

-Lead design for manufacturability (DFM) and design transfer initiatives in collaborationwith development teams.

-Use structured problem-solving techniques and statistical methods for data drivenanalysis and decisions.

-Manages process and equipment validations for new and existing product lines.


-Bachelor’s degree (B.S.) in Mechanical, Manufacturing, Industrial or related Engineeringdiscipline is required.

-Master’s degree preferred


-7+ years hands on experience in process and project engineering

-5+ years of experience in new product development and/or integration of newmanufacturing processes.

-3+ years of management experience

-Experience working within FDA 21 CFR 820 Quality system is required

-Experience leading teams in product design, manufacturing and tool design

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