No more applications are being accepted for this job
- Bachelor's degree in Engineering is required.
- knowledge of FDA CFR 820, ISO 13485, and ISO 9000 requirements; ISO 13485 Lead Auditor certification is highly desired.
- minimum 5 years of relevant experience, including previous involvement in quality auditing, particularly supplier audits. documentation, communication, and problem-solving skills are highly desirable.
- Proficient in oral and written communication in English.
location: Cleveland, Mississippi
job type: Contract
salary: $ per hour
work hours: 8am to 4pm
education: Bachelors
responsibilities:
- Collaborate with suppliers to address identified issues and find effective solutions.
- Prepare comprehensive written reports and effectively communicate audit results to both auditees and management.
- Oversee and ensure timely implementation of Supplier Corrective Action Reports (SCARs).
- Provide engineering support for nonconforming material (NMR) and Return Material Authorization (RMA) issues.
- Update and enhance Supplier files to support current operations and business development activities.
- Revise and enhance the Supplier Nonconformance (SNC) process.
- Ensure proper maintenance and documentation of supplier files.
- Generate and present supplier metrics to management.
- Lead the supplier approval process, assessing manufacturing and Quality Systems capabilities and associated risks.
- Develop improvement plans for Critical to Quality (CTQ) suppliers.
- Supervise personnel to optimize Incoming Inspection cycle time.
- Develop problem-solving strategies and collaborate with Manufacturing and Quality Engineers to reduce Material Review Board (MRB) inventory.
- Conduct component characteristic analysis to determine changes in inspection status.
qualifications:
- Experience level: Experienced
- Minimum 5 years of experience
- Education: Bachelors (required)
skills: - Quality
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
Applications accepted on ongoing basis until filled.
Quality Engineer - Cleveland, United States - Randstad USA
Description
job summary:We have a Contract opportunity with one of the leading Medical device manufacturers in the country. If you're looking for a new opportunity please apply.
Requirements: