set a job alert
Get notified by mail on all jobs that match your preferences.
filters
- 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: 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 supjob 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: 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 sup
- job summary: Continuous Improvement Specialist for a leading manufacturer based in Hattiesburg, MS. This role is responsible to develop, Train and Implement Standard Work for all levels of employees in all departments. To be considered - must have BS Degree with Continuous Improvement experience within a manufacturing environment. This is a long term contract opportunity. Per diem is available. APPLY NOW! Required Qualifications: B.S Degree (Enginjob summary: Continuous Improvement Specialist for a leading manufacturer based in Hattiesburg, MS. This role is responsible to develop, Train and Implement Standard Work for all levels of employees in all departments. To be considered - must have BS Degree with Continuous Improvement experience within a manufacturing environment. This is a long term contract opportunity. Per diem is available. APPLY NOW! Required Qualifications: B.S Degree (Engin
