A global leader in medical devices is seeking for an Engineering Associate Specialist to join their headquarters in Irvine! This is a contract role.
The Engineering Associate Specialist is responsible for providing technical support to the Engineering, Quality, and Operations team with the evaluation of requests for any additional changes of work orders.
Document, support and create: testing assembly instructions, Engineering Change Request (ECRs) and other documentation.
Support various tasks including corrections of work order documents and other corrections to part/drawing/documents.
Assist with elimination of any backlog of Engineering Change Requests for various engineering projects.
Work in cross functional team to review and update existing product design documents to ensure compliance internally and externally
Complete Engineering Change Requests for process and product design review
Assist with any remaining manufacturing remediation activities (e.g. IQ/OQ/PQ) as needed
We are an equal opportunity employer and make hiring decisions based on merit. Recruitment, hiring, training, and job assignments are made without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, or any other protected classification. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.