SI-BONE is a fast-growing, publicly traded medical device company that is an industry pioneer in minimally invasive sacropelvic solutions. The Manufacturing Engineer will create, improve, implement and document processes and procedures to manufacture, package and label the company’s products.
Requirements
- Mechanical engineering experience in a medical device environment
- Experience working with CAD, Solid Works, Pro E, etc.
- Supplier sourcing, evaluation and management
- Creation and development of standard operation procedures, work instructions, inspections documentation, change controls and visual aids
- Collaboration with peers to design and develop supply chain manufacturing processes
- Support Engineering Change Notice (ECN) and related Material Review Board (MRB) activities
- Participation in cross-functional teams with a focus on product packaging technologies, testing, validations and labeling
- Assistance in the evaluation of returned materials/products
- Support and adherence to company policies, procedures, goals and objectives, QSR/FDA regulations
Benefits