QA Specialist III job in Des Plaines, IL
Vacancy has expired
Des Plaines, IL CorTech LLC
| Job Ref: | 344775 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 37.86/Per Hour |
| Remote: | No |
Location |
|
| City: | Des Plaines, IL |
| Post Code: | 60018 |
| Map: |
|
Description |
|
|
CorTech is seeking to hire a QA Specialist III for our client in Des Plaines, IL! Benefits Available! Weekly Pay! $37.86/Hour Start Time (AM/PM) 8am End Time (AM/PM) 5pm This position is NonExempt. Hours over 40 will be paid at Time and a Half. Assures the quality of manufactured products and processes per standard operating processes(SOP'S) and GMP (Good Manufacturing Practices). BS degree and/or 5+ years equivalent experience This is an onsite role Job Description: Responsible for activities related to supplier evaluation and supplier performance monitoring and improvements. Contributes to the development, establishment and maintenance of supplier quality engineering methodologies, systems and practices which meet Client and regulatory requirements. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success for assuring high product quality and meeting business needs. Main Responsibilities ? Manage reagent and commodity supplier investigations, action plans, effectivity checks, and other documentation. ? Approves components for use in products by driving Production Part Approval activities ? Supports supplier change notification process and process improvement efforts. ? Supports the evaluation and development of Supplier Quality Agreements. ? Supports incoming Non-Conforming Material Report (NCMR) activities and related record evaluation with notifications. ? May support molding qualifications. Minimum Requirements: Bachelor?s degree in Life Science; Engineering; or closely related discipline is required OR relevant combination of education or experience. At least 7 years work experience in Quality or related field experience; Has a history of completing successful projects and driving positive compliance outcomes. Preferred: ? Bachelor's or master?s degree in one of the following Engineering disciplines: Chemical, Electrical, Bio-medical, or Mechanical ? 7+ years of relative professional work experience in Medical Device Quality or in a regulated industry (Ex.: Automotive) ? Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971 ? Strong technical writing skills; Polished verbal and written communication skills and experience with Trackwise. | |
ref: (344775)
1082 days ago
Back to search results