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Quality Assurance (QA) Lead Coordinator

United States, Port Neches · Job Posted May 16, 2026
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Job Description

Airswift is seeking an Quality Assurance Lead to work within our client's chemical facility in Port Neches, TX for a 6-month+ assignment with potential for going direct with the client.

Job Responsibility

  • Lead the implementation and maintenance of GMP practices across all operations
  • Ensure compliance with quality and safety standards, including ISO 9001, ISO 22716, ISO 14001, ISO 45001, RSPO, BRCGS, EXCiPACT, FSSC22000, EFfCI, Kosher, and Halal
  • Maintain current certifications and implement new ones aligned with business strategy
  • Develop and deliver training programs on quality standards and GMP requirements
  • Update and control the Document Management System
  • Develop and manage annual internal and external audit programs
  • Facilitate and lead audits, ensuring compliance with scope, objectives, and timelines
  • Oversee audit execution, review reports, and ensure closure of findings
  • Maintain a qualified audit team and engage external consultants as needed
  • Monitor audit trends and share insights with leadership
  • Manage the execution of the Validation Master Plan
  • Develop validation protocols for equipment, systems, cleaning, and CCPs
  • Ensure compliance with validation programs and revalidation requirements
  • Investigate non-conformities and perform root cause analysis
  • Lead local Quality & Product Safety Committees
  • Coordinate management reviews, recalls, and non-conformance teams
  • Define KPIs and drive continuous improvement initiatives
  • Implement and train risk analysis methodologies (FMEA & HACCP)
  • Qualify and monitor suppliers, supporting supplier audits
  • Manage customer quality documentation and agreements
  • Monitor regulatory developments, including FDA Foreign Supplier Verification Program

Requirements

  • Subject Matter Expertise in GMP Standards (EXCiPACT, FSSC22000, BRCGS, etc.) with proven ability to lead GMP programs
  • Hands-on Experience in Facilitating and Leading Audits (internal and external)
  • Experience in Chemical Manufacturing Processes with strong understanding of quality and safety requirements
  • Minimum [X] years of experience in quality assurance within chemical or pharmaceutical manufacturing
  • Strong knowledge of ISO standards and risk management methodologies (FMEA, HACCP)
  • Excellent leadership and communication skills
  • Ability to manage multiple projects and priorities
  • Proficiency in document control systems and audit management tools
  • Bachelor’s degree in Chemistry, Chemical Engineering, Quality Assurance, or related field

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