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Added 1 min ago
Service Manager
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4 years of auto service technical experience.
Added 1 min ago
Program Manager - Hybrid
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Operations - Process Manager - Sr
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Group Product Manager, Privacy
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Phigenics

Laboratory Quality Manager

Warrenville, IL, United States

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Job details

Experience: 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)
Posting language: English
Posted: Nov 3, 2026

Original job description

Position Title: PASL Quality Manager

Reporting To: Senior Director of Operations

Location: Warrenville, IL (Phigenics Analytical Services Laboratory – PASL)

Summary

Phigenics Analytics Services Laboratory (PASL) operates two environmental testing laboratories, who perform water microbiology and chemistry testing in support of building water management programs. Both sites are accredited under TNI/NELAP and are seeking to gain ISO/IEC 17025:2017 accreditation.

The PASL Quality Manager owns and leads the Quality Management System (QMS) for both laboratories, ensuring its improvement, continued maintenance, and alignment with ISO/IEC 17025 and all applicable accreditation, regulatory, and customer requirements. As Quality Manager, this individual has the authority and freedom to identify quality issues, initiate corrective action, and ensure the integrity of laboratory operations. This role leads the accreditation program and supervises and develops the quality team.

Job Duties

Own, implement, and continually improve the PASL Quality Management System in full conformance with ISO/IEC 17025:2017, TNI Standard 2016, and any additional internal or external standards
Serve as PASL's primary point of contact with the accrediting body (e.g., A2LA, ANAB) for all accreditation matters, including scheduling, hosting, and responding to on-site assessments and surveillance audits
Plan and execute the annual internal audit program across both PASL locations; lead and support the external accreditation audits
Lead the Corrective Action and Preventive Action (CAPA) process, including root cause analysis, effectiveness verification, and timely closure of findings
Own the management review process, compiling quality metrics, audit results, customer feedback, and QMS performance trends for review with laboratory and company leadership
Oversee document control for the quality manual, SOPs, forms, and records across chemistry, microbiology, logistics, and manufacturing workflows; ensure annual review and version control
Direct the laboratory equipment calibration and preventive maintenance program, ensuring metrological traceability for all measurements within the scope of accreditation
Oversee measurement uncertainty, budgets, and support method validation/verification for new or revised test methods prior to introduction into the scope of accreditation
Design, administer, and evaluate the laboratory's proficiency testing (PT) and interlaboratory comparison program; investigate and resolve any unacceptable PT performance
Recruit, train, mentor, and manage performance of PASL quality specialist(s); ensure staff competency assessments and quality training records are current and documented
Maintain and review the PASL Safety Manual annually and support execution of the PASL Safety Program in partnership with the Phigenics safety team
Maintain working knowledge of PASL software and laboratory systems (e.g., ATL Titan LIMS, Bio-Rad CFX Manager, EndoScan-V, FedEx Ship Manager) and ensure quality data integrity within these systems
Travel periodically between the Warrenville, IL and Fayetteville, AR laboratories as needed to maintain consistent quality practices across both sites

Education and Experience

Bachelor's 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 laboratory's 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

Accountabilities

Safety is our first priority. No accident is acceptable
Implement and maintain PASL's 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 PASL's laboratory software and systems

Phigenics LLC is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, creed, color, religion, alienage or national origin, ancestry, citizenship status, age, disability or handicap, sex, marital status, veteran status, sexual orientation, arrest record, or any other characteristic protected by applicable federal, state or local laws. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

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