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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