Quality Engineer
Location: Kalamazoo, Michigan
About Our Client:
Accepting no less than the absolute best, our client has climbed to the top, gaining a reputation for both excellence and satisfaction. Working at this company will give you the opportunity to work with some of the top technical professionals in the industry who are bringing cutting-edge products to forefront. Offering results-driven people a place where they can truly make a difference on a daily basis, this is an opportunity you will not want to miss!
Key Responsibilities:
- Developing and implementing methods and procedures for process control, process improvement, testing, and inspection to ensure product quality.
- Designing and installing sophisticated testing equipment and performing product testing and analysis to validate functionality and minimize defects.
- Analyzing reports and defective products to identify trends, root causes, and recommending corrective actions.
- Collaborating with supplier representatives to resolve quality issues, ensuring effective corrective actions are implemented, and contributing to supplier quality improvement initiatives.
- Participating in validation activities to ensure compliance with industry standards and regulatory requirements.
- Supporting cross-functional teams in identifying and mitigating quality risks throughout the product lifecycle.
- Maintaining detailed documentation of quality procedures, findings, and improvements to support audit readiness and continuous improvement.
Qualifications:
- Degree required (Engineering or a related technical field preferred).
- Strong analytical and problem-solving skills with the ability to identify root causes and implement effective solutions.
- Excellent written and verbal communication skills for reporting findings and collaborating with cross-functional teams.
- Ability to manage multiple tasks and prioritize in a fast-paced, team-oriented environment.
- Knowledge of quality systems and regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820).
- PPAP (Production Part Approval Process) experience is preferred.
- Experience working with medical devices or in a regulated manufacturing environment is a plus.
- Familiarity with tools such as FMEA, CAPA, and statistical process control is preferred.
- NO C2C CANDIDATES
Interested Candidates please apply on our website at https://jobs.jblresources.com.
For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com.
JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be.
**JBL is an Equal Opportunity Employer and E-Verify Company
