What are the responsibilities and job description for the Manufacturing Process Engineer position at Powerwell?
Company Overview
">Powerwell is a leading manufacturer in the medical device industry, committed to delivering high-quality products while driving continuous improvement. As a Process Engineer II, you will play a critical role in maintaining operational efficiency and driving innovation in our fast-paced manufacturing environment.
Job Summary
We are seeking an experienced Process Engineer II to join our team at Powerwell. This exciting opportunity allows you to build a long-term career with a stable and innovative organization, offering competitive pay and comprehensive benefits from day one of employment.
Key Responsibilities
- Create and manage routers, bills of materials, and inspection instruction sheets to ensure seamless production processes.
- Utilize statistical process control (SPC) methods to drive process improvements, reducing defects and increasing efficiency.
- Design and refine inspection and gauging methods, determining appropriate inspection frequencies to maintain quality standards.
- Collaborate on new product development through design reviews, pre-production planning, and manufacturing coordination.
- Assist in addressing customer complaints by implementing corrective and preventive actions, ensuring timely resolution and satisfaction.
- Identify opportunities for process optimization and implement innovative solutions, driving continuous improvement in our manufacturing operations.
Required Skills and Qualifications
- Bachelor of Science in Engineering, preferably in a related field such as mechanical engineering or industrial engineering.
- Proficiency with AutoCAD, SolidWorks, or similar software, with experience in designing and refining manufacturing processes.
- Familiarity with statistical tools such as control charts and capability analysis systems, with knowledge of quality management systems and tools.
- 3 years of engineering experience, preferably in CNC machining or the medical device industry, with experience in validation processes, Production Part Approval Process (PPAP), or Advanced Product Quality Planning (APQP).
Benefits
- Competitive salary and comprehensive benefits package, including health coverage, company-paid insurance, retirement plan, and paid time off.
- Opportunities for professional growth and development, working with a talented team of professionals in a thriving and innovative industry.
- A supportive work environment, with a focus on collaboration and teamwork, to drive success and achieve goals.
