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- Follow up on supplier audits to demonstrate supplier controls required by FDA CFR 820, ISO 13485, and ISO 9000.
- Works with suppliers to find solutions to identified problems.
- Create written reports and communicate the results clearly and effectively to the auditee and management.
- Manage and insure timely implementation of supplier Corrective Action Reports SCARs.
- Knowledge of FDA CFR 820, ISO 13485 and ISO 9000 requirements, strongly desired ISO 13485
- Lead Auditor certification. B.S Degree in Engineering required.
- 5+ year qualifying experience, including previous experience with quality auditing, specifically supplier audits.
- Excellent documentation, communication, and excellent problem-solving skills desirable.
- To be immediately considered, please send an updated version of your resume to
- Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry – even if this position doesn't work out, you're still in the Kelly network. That means our team of expert recruiters will have access to your profile, making your opportunities limitless.
Supplier Quality Engineer - Cleveland, United States - Kelly Science, Engineering, Technology & Telecom
Description
Hello, my name is Daniel, and I am a recruiter with Kelly Services. One of our prominent clients is seeking a Supplier Quality Engineer in Cleveland, MS.
Responsibilities:
Qualifications:
Important information:
What happens next: