What are the responsibilities and job description for the Manufacturing Process Improvement Specialist position at Powerwell?
Company Overview
Powerwell is a leading recruitment firm that connects top talent with exciting career opportunities in the medical device industry. We are currently recruiting for a Process Engineer II to join our client's team in Indiana.
Our client is a highly respected company with a strong commitment to innovation and quality. As a Process Engineer II, you will be responsible for improving manufacturing processes, supporting product development, and ensuring the production of high-quality products.
Salary
This is an excellent opportunity to build a long-term career with a stable and innovative organization. The role offers competitive pay and comprehensive benefits from day one of employment.
Job Description
As a Process Engineer II, your key responsibilities will include:
Required Skills and Qualifications
To be successful in this role, you will need:
Benefits
As a member of our team, you can expect:
Others
If you're passionate about improving manufacturing processes and contributing to a fast-paced environment, this is an excellent opportunity to take your career to the next level.
Powerwell is a leading recruitment firm that connects top talent with exciting career opportunities in the medical device industry. We are currently recruiting for a Process Engineer II to join our client's team in Indiana.
Our client is a highly respected company with a strong commitment to innovation and quality. As a Process Engineer II, you will be responsible for improving manufacturing processes, supporting product development, and ensuring the production of high-quality products.
Salary
This is an excellent opportunity to build a long-term career with a stable and innovative organization. The role offers competitive pay and comprehensive benefits from day one of employment.
Job Description
As a Process Engineer II, your key responsibilities will include:
- Create and manage routers, bills of materials, and inspection instruction sheets.
- Utilize statistical process control (SPC) methods to drive process improvements.
- Design and refine inspection and gauging methods, while determining appropriate inspection frequencies.
- 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.
- Execute validation protocols and participate in the material review process.
- Identify opportunities for process optimization and implement innovative solutions.
Required Skills and Qualifications
To be successful in this role, you will need:
- A Bachelor of Science in Engineering.
- Proficiency with AutoCAD, SolidWorks, or similar software.
- Familiarity with statistical tools such as control charts and capability analysis systems.
- Knowledge of quality management systems and tools such as Failure Mode & Effects Analysis (FMEA).
- 3 years of engineering experience, preferably in CNC machining or the medical device industry.
- Experience with validation processes, Production Part Approval Process (PPAP), or Advanced Product Quality Planning (APQP) is a plus.
Benefits
As a member of our team, you can expect:
- Health coverage: Medical, dental, and vision plans.
- Company-paid insurance: Short-term disability, long-term disability, life insurance, and accidental death & dismemberment (AD&D).
- Retirement plan: 401(k) with 50% company match up to 3%, starting the first of the month after 30 days of employment.
- Paid time off: Generous vacation and holiday schedule.
Others
If you're passionate about improving manufacturing processes and contributing to a fast-paced environment, this is an excellent opportunity to take your career to the next level.
