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Listed below are the top 10 out of 123 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Irvine, CA
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Fashion Industry Employer - Huntington Beach, CA US
Coordinate inline bulk production for Apparel and Accessories department Work closely with Merchandising, Domestic/International Sales Ops, Logistics, ...
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For your reference, we have included the original job posting below.
Doccument Coordinator - Medical Device Manufacturing
Job Number:
23653754
Company Name:
CORESTAFF
Job Location:
Irvine, CA US
Job Category:
Management & Business
Doccument Coordinator - Medical Device Manufacturing
Title Doccument Coordinator - Medical Device Manufacturing Job Category Information Tech City Irvine, State CA Location Irvine, CA Zip Code 92612 Salary Job Type Direct Hire Req Education Date Posted Description
Summary: This position works cross-functionally to support efforts to define, setup and maintain an automated Quality training system. Maintains records management for Quality Systems and is responsible for backup support for Document Control.
Essential Duties and Responsibilities: · Tracks training compliance and reports status of company-wide training compliance. · Coordinates training compliance for satellite employees. · Processes protocols and reports, scans and uploads document to MasterControl. · Supports user requests for documentation and updates satellite areas within facility. · Orders external standards, maintains tracking system and coordinates review with users. · Maintains records in the document control storage room in a state of audit readiness. · Responsible for providing backup support for coordinating document change orders (DCO), coordinates review and approval. · Responsible for the retention of Risk Management documents. · Performs filing and scanning of quality system documentation. · Other duties as assigned by the supervisor. Requirements
· Hgh school diploma required, Bachelors Degree preferred. · xperience in a pharmaceutical or medical device manufacturing environment desired. · Strong computer skills (Microsoft Office products including Word, Excel and Powerpoint) required. · Possess strong verbal and written communications · Knowledge of ISO and GMP regulations desired. · Knowledge of documentation control requirements for medical device manufacturing to meet FDA and ISO 13485 regulations desired. · Must be detail-oriented and posses strong organizational and time management skills with the ability to prioritize and manage completion of multiple tasks/projects with company personnel. · Strong interpersonal skills, with the ability to communicate effectively with all levels of staff including non-technical and technical personnel. · Must be quality oriented and willing to promote quality standards. · Experience with electronic documentation & training system a plus. Boilerplate
