Bachelors degree in Chemistry, Microbiology, Biology, or a related scientific field Minimum of 5 years of laboratory quality experience, including direct, hands-on experience implementing and maintaining a Quality Management System under ISO/IEC 17025 (required) Prior experience serving as a laboratorys designated Quality Manager, or in an equivalent role under an ISO/IEC 17025 accreditation, strongly preferred ISO/IEC 17025 Internal Auditor or Lead Assessor training/certification preferred; ASQ Certified Quality Auditor (CQA) or similar credential a plus Demonstrated experience leading internal and external audits, CAPA programs, and management review processes Working knowledge of measurement uncertainty, method validation/verification, and proficiency testing programs Prior people-management experience, with the ability to train, coach, mentor, set clear expectations, and support their development Strong technical verbal and written communication skills, including policy and procedure development and audit reporting Strong time management, attention to detail, and interpersonal skills (team player) Ability to work overtime occasionally, sometimes with little or no notice Knowledgeable in the use of computers - MS Office, LIMS and other laboratory software, and shipping programs. No accident is acceptable Implement and maintain PASLs ISO/IEC 17025 accreditation and overall QMS conformance Ensure effective execution of internal and external audit programs and timely CAPA closure Develop, maintain, and improve PASL SOPs, quality documentation, and workflow processes Lead and develop the PASL Quality team and facilitate quality-related training Oversee the laboratory safety program and related procedures Maintain the equipment calibration and preventive maintenance program Own data integrity and quality within PASLs laboratory software and systems.