Document Control Specialist Jobs in California

Job Title: QA Document Control Admin Company: Volt Workforce Solutions Location: Irvine, CA Description: Volt has partnered with a leading company in Rancho Santa Margarita to help identify an experienced QA Document Control Admin for an immediate 3 - 5 month temporary opportunity. Our client is a mid size company that performs pharmaceutical manufacturing. In this role, you will be responsible for; performing word processing of documents, drafts and revisions submitted for proofreading; maintaining accurate and secured electronic and hard copy files of QA documents; assigning document numbers to procedures; assigning approval routing; maintaining the executive filing system; and ensuring GMP/ISO compliance and continuous improvement in all document control activities. Position pays between $15 - 16/hr. Submit resume today for immediate consideration. Volt Workforce Solutions is an Equal Opportunity Employer with a commitment to fostering diversity in the workplace. For more job opportunities with Volt please visit our web site at http://jobs.volt.com .Requirements: Qualified candidates will possess a minimum of 2 - 3 years experience in document control, preferably within the medical manufacturing industry. Training in GMP/ISO is highly preferred. Must possess excellent verbal and written communication skills and be proficient in MS Office.

Job Title: Temporary Document Control Specialist Company: Location: Los Angeles, CA Description: Spectrum Labs, a high-tech leading supplier of biofiltration devices, is seeking a Temporary Document Control Specialist to join our growing team. Responsibility and authority: ? Manages engineering and quality document control system. ? Maintains fully-automated system to electronically store, retrieve, update, and distribute engineering and manufacturing documentation. ? Assists in the development of all types of company documentation. ? Assists in Scheduling and managing ISO, quality, and documentation meetings. ? Ensures timely and accurate revisions to and distributions of pending and approved company documentation relating to policies, procedures, processes and products. ? Ensures accurate retention of company documentation relating to policies, procedures, processes and products. ? Participates in project planning with the development teams and supports team efforts as needed. ? Conducts/participates in internal audits. ? Supports facility audits conducted by customers and regulatory agencies. ? Generates/manages Document Change Orders (DCO). ? Procures signatures on DCOs. ? Enters bills of materials and modifies BOM?s as required by MIS. ? Assists Engineering with AutoCAD changes. __________________________ Minimum qualifications and experience requirements: ? Minimum AA degree or equivalent experience. ? 2+ years of experience in Document Control. ? Familiar with ISO 9001, computer literate, knowledge of engineering and medical devices. __________________________ Delegation of Duties during absence (indicate position title): ? To be determined by the Director of Quality Assurance and Regulatory Affairs Duration of the job - June 2010 to November 2010