Quality Engineer
Charlotte, South
Medical Device Manufacturing
$75,000 - $85,000
Start date: ASAP
I’m working with a medical device manufacturing company who are on the lookout for a quality engineer to join their team in South Charlotte North Carolina.
This is a medium sized manufacturing company, but they are investing heavily in their staff and their infrastructure to be able to grow into a well-known household brand.
This company already has a global presence and works with a wide array of clients themselves. These vary from small startups to some of the biggest names in the world, and you could be a part of this growing company.
If you want to become a part of a team that invests in it’s staff to improve the overall company, that has clear paths of progression to promotions and a company that has committed to an impressive amount of growth in the next 5 years then this could be the company for you.
Job responsibilities:
· Handle change control tasks as needed.
· Lead analysis, inspection, design, testing, and integration to ensure product quality.
· Use statistical process control (SPC) methods to analyze data and evaluate processes and changes.
· Help develop new ways to solve problems found during manufacturing or quality checks.
· Uphold and implement quality standards, inspection processes, testing methods, quality plans, and related reports.
· Create and/or review fixture designs.
· Keep a log of part changes or BOM for fixtures.
· Develop and track quality KPIs as directed by Quality Management.
· Present data to management using Excel, PowerPoint, Minitab, or Power BI.
· Support product/process assessments, CAPA, validations, and continuous improvement activities.
· Report quality issues, trends, and losses to management.
· Complete MMDS & SPoT processes for new materials and products.
· Create, revise, and update quality-related documents.
· Assist with risk management activities.
· Help with external and internal audits.
· Perform other duties as assigned.
Requirements:
· Bachelor’s degree in engineering or related field, or at least 3 years of experience with an Associate degree.
· 0-3 years of experience in high-volume, regulated manufacturing in an engineering role.
· Good understanding of statistics and statistical process control.
· Familiar with various inspection control methods, techniques, and documentation.
· Strong computer skills, including QA applications, word processing, spreadsheets, and databases.
· Able to record, interpret, and present data in different formats.
· Skilled in identifying problems, collecting data, and drawing conclusions.
· Experience with CAD/SolidWorks.
· Knowledge of Six Sigma, lean, and Quality Management Tools.
· Able to read and understand technical drawings and documents.
· Experience with CMM programming.
· Able to work independently and take initiative.
· Excellent communication, analytical, troubleshooting, and interpersonal skills.
· A team player who can also work independently.
If you feel like you would be a good fit for this position please apply for immediate consideration.
Job Type: Full-time
Pay: $80,000.00 - $100,000.00 per year
Benefits:
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
Schedule:
Education:
Experience:
- Medical Device Manufacturing: 1 year (Required)
- Quality Engineering: 2 years (Required)
Ability to Commute:
- East Lansing, MI 48824 (Required)
Work Location: In person