Full-Time
Manufacturing Engineer II
Posted on 4/5/2024
Develops healthcare technologies for vascular conditions
Compensation Overview
$86,340 - $113,700Annually
Junior
Roseville, CA, USA
- Bachelor's degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree with 1+ years relevant engineering experience
- Engineering experience in a manufacturing environment recommended, medical device industry preferred
- Excellent written, verbal, and interpersonal communication skills required
- Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing processes desired
- Proficiency in Word, Excel, PowerPoint, Access, and other computer applications required
- Solve complex problems and implement innovative solutions
- Execute detailed root cause analysis and recommend vetted solutions
- Communicate and explain problems and solutions cross-functionally and interdepartmentally
- Approach problems from a detail-oriented perspective
- Suggest independent recommendations for project approach, scope, and tactics
- Support production; Creating and maintaining product and process documentation; Monitor process and equipment performance and identify and implement process improvement activities to increase/optimize yield, efficiency, and/or throughput
- Design fixtures, acquire off-the-shelf tooling and equipment, and implement new fixturing on the production line
- Test processes, equipment, raw materials, and product. Perform process validations
- Plan, schedule, conduct, and coordinate detailed phases of engineering work as part of a project or as a total project
- Develop specifications of a product, process, or piece of equipment
- Develop, characterize, and optimize processes using statistical techniques and engineering knowledge and experience
- Coordinate with the appropriate suppliers and other external resources needed in developing and implementing process improvement plans
- Participate in project planning and scheduling
- Train assemblers, quality control and technicians, as necessary, on processes, equipment, and documentation
- Adhere to the Company’s Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures
- Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company
- Ensure other members of the department follow the QMS, regulations, standards, and procedures
- Perform other work-related duties as assigned
Penumbra, Inc. excels in pioneering healthcare technologies specifically designed for neuro and peripheral vascular conditions. This involves a focus on stroke revascularization and embolization, with leading products like the REAL Immersive System and ACE Reperfusion Catheters that underline their commitment to top-tier, patient-focused innovations. Their dedication to leveraging cutting-edge technology in medical solutions makes it an outstanding workplace for professionals eager to impact critical care positively and advance in the fast-evolving healthcare sector.
Company Stage
IPO
Total Funding
$3.4M
Headquarters
Alameda, California
Founded
2004