QA Documentation Specialist-I

Integrated Resources, Inc

  • Foster City, California
  • 9 days ago
  • Full-time
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Skills

  • Auditingunmatched
  • Biotech and Pharmaceuticalunmatched
  • Clinical Researchunmatched
  • Corporate Policiesunmatched
  • Corrective Actionunmatched
  • Document Managementunmatched
  • Documentationunmatched
  • FDA Requirementsunmatched
  • Identify Issuesunmatched
  • Information Technology & Information Systemsunmatched
  • Information/Data Security (InfoSec)unmatched
  • Internal Auditunmatched
  • Leadershipunmatched
  • Maintain Complianceunmatched
  • Product Testingunmatched
  • Quality Assuranceunmatched
  • Quality Assurance Methodologyunmatched
  • Quality Controlunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Rehabilitation Nursingunmatched
  • Risk Managementunmatched
  • Root Cause Analysisunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Testingunmatched
  • United States Department of Agriculture (USDA)unmatched

Description

QA Documentation Specialist-IIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob Title: QA Documentation Specialist-IDuration: 6 MonthsLocation: Foster City, 94404Responsibilities:Specializing in compliance and regulatory affairs in the pharmaceuticals & biologics sectors.Meticulous Quality Assurance Auditor with over 5 years of experience leading QA/QC programs to drive strict compliance with diverse regulatory requirements, including FDA, USDA, International Standards, safety regulations, and industry-specific governance.Drive compliance with multiple regulatory requirements, International Standards, and company policies and procedures by auditing records and reports, inspecting processes and documents, reviewing SOPs, and independently monitoring all facilities, operations, personnel, and materials.Adept at managing and mitigating risk, using a proactive approach to identify issues and collaborate with leaders to create and implement corrective action.Skilled in root cause analysis, multi-phase product sampling and testing, and ensure compliance of equipment and facility inspections.Carefully document testing and audit results in Quality Assurance Logs and process records, and shared test results with production workers, supervisors and managers to identify and implement solutions.Extensive experience in process, internal audit, and documentation approval to ensure the availability and security of historical data and records.Utilized Trackwise as Electronic Document management system.Qualifications3+ years of relevant experience in a regulated industry and an AS degree.EDMS experience is must

Numbers & Facts

LocationFoster City, California
Job TypeFull-time

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