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Quality Assurance Specialist - FDA Manufacturing

Rose International

  • Mebane, North Carolina
  • 4 days ago
  • $27.10–$27.50 Per Hour
  • Temporary
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Skills

  • Administrative Skillsunmatched
  • Check Processingunmatched
  • Communication Skillsunmatched
  • Computer Skillsunmatched
  • Corrective Actionunmatched
  • Cross-Functionalunmatched
  • Data Collectionunmatched
  • Detail Orientedunmatched
  • Documentationunmatched
  • Documentation Reviewunmatched
  • Establish Prioritiesunmatched
  • FDA (Food and Drug Administration)unmatched
  • GMP (Good Manufacturing Practices)unmatched
  • ISO (International Organization for Standardization)unmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Media Productionunmatched
  • Microsoft Officeunmatched
  • People Managementunmatched
  • Problem Solving Skillsunmatched
  • Procedure Developmentunmatched
  • Procedure Implementationunmatched
  • Process Qualityunmatched
  • Product Supportunmatched
  • Production Supportunmatched
  • Production Systemsunmatched
  • Quality Assuranceunmatched
  • Quality Controlunmatched
  • Quality Engineeringunmatched
  • Quality Metricsunmatched
  • Quality System Requirements (QSR)unmatched
  • Realtime Communicationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Sample/Specimen Processingunmatched
  • Sampling Inspectionunmatched
  • Secondary Schoolunmatched
  • Support Documentationunmatched
  • Team Playerunmatched
  • Technical Supportunmatched
  • Time Managementunmatched

Description

Job TitleJob Description Required Education: Bachelor's degree, or High School with 4 years' additional experience in manufacturing or quality assurance Required Skills and Experience: Minimum of 2 years' experience in manufacturing or quality in an FDA-regulated or ISO 13485 environment Basic knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) Experience with inspection, documentation review, or production support activities Strong attention to detail and ability to identify errors and nonconformances Ability to work independently and in a team environment in a fast-paced production setting Effective communication skills for interaction with production and cross-functional teams Basic computer proficiency (e.g., Microsoft Office) Ability to assess the immediate quality impact of events observed on the production floor and support appropriate escalation, containment, and documentation in accordance with established procedures and quality system requirements Sound independent judgment in identifying potential compliance or product quality concerns, prioritizing issues, and taking appropriate action within defined responsibilities while recognizing when escalation is needed Strong working knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) in a regulated manufacturing environment Attention to detail and ability to identify documentation errors, process deviations, and nonconforming conditions in real time Effective communication and collaboration skills for working with Manufacturing, Quality Control, Engineering, Maintenance, and other cross-functional teams Ability to perform documentation review and basic fact gathering to support investigations and issue resolution Ability to work effectively in a fast-paced production environment while maintaining a high standard of compliance, accuracy, and responsiveness Preferred Skills and Experience: Familiarity with sampling plans and inspection standards Experience supporting production floor quality activities Basic understanding of nonconformance processes Responsibilities: Provide daily, hands-on quality support on Liquid Media production lines Assist as needed to verify line setup and line clearance activities Perform in-process quality checks and spot inspections to ensure adherence to procedures and specifications Conduct real-time review of production documentation for accuracy, completeness, and legibility Ensure compliance with GDP requirements and identify documentation errors for correction Monitor and escalate recurring documentation issues to supervision for corrective action Detect and document nonconforming conditions during production and inspection activities, and initiate containment actions Perform preliminary fact gathering to support investigations Escalate complex issues to Quality Engineers or appropriate technical functions Support investigations through documentation review and data collection Partner with Manufacturing, Engineering, Maintenance, and Product Support to resolve quality-related issues Provide guidance to production associates on quality requirements and documentation expectations Coordinate or assist with sample preparation and submission to the QC laboratory Serve as the on-floor quality representative to ensure compliance with procedures and regulatory requirements Promote awareness of quality standards, defect prevention, and GDP compliance Escalate risks and quality concerns in a timely manner**Only those lawfully authorized to work in the designated country associated with the position will be considered.****Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.**

Numbers & Facts

LocationMebane, North Carolina
Job TypeTemporary
IndustryStaffing/Employment Agencies
Salary$27.10–$27.50 Per Hour
Company Size2,500 to 4,999 employees
Websitehttps://www.roseint.com/

About Company

Founded in 1993 by Sue Bhatia, Rose International is one of the nation's leading minority- and woman-owned providers of Staffing and Total Talent Solutions. We serve companies in all 50 states and employ thousands of people across the country.

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