Quality Assurance Specialist
Core
Design, develop, and implement internal auditing programs and procedures to ensure adherence to ISO/IEC 17025:2017 accreditation and GLP requirements in a commercial laboratory setting.
Role type
Quality Systems Specialist (Laboratory Auditing & Compliance)
Builds
Internal audit programs, corrective action plans, supplier quality evaluations, and compliance documentation for ISO 17025/GLP/GMP standards.
Domain
Life Sciences / Laboratory Quality Assurance / Regulatory Compliance
Deliverable
dashboards & analysis
Required skills
Internal auditing, GLP inspections, non-conformance investigation, corrective action tracking, supplier quality evaluation, equipment qualification record management, proficiency testing review, refresher training coordination, quality metrics reporting, technical instrumentation calibration, MS Office proficiency, written and spoken English proficiency.
Preferred skills
Experience in FDA/USDA regulated sectors, familiarity with electronic submission systems and document management systems.
Responsibilities
Schedule and perform internal audits; Participate in external audits; Review and investigate non-conformances and client complaints; Issue and monitor corrective actions; Evaluate supplier quality; Review, approve, and maintain equipment qualification records; Perform administrative tasks related to quality policy implementation.
Seniority
Mid-level, hands-on IC