GLP Vendor Oversight and QA Lead

CSL; King of Prussia (PA); On-site; USD 120,000 - 180,000; Full time

Job summary

CSL is seeking a GLP Vendor Oversight and QA Lead in King of Prussia, PA to own external partner quality programs. You will drive risk-based oversight, audits, and continuous improvement across CROs and laboratories to ensure GLP, GCP, GMP compliance and data integrity.

Responsibilities include establishing Quality Agreements, KPIs, audit readiness, and collaboration with Nonclinical Development, Legal and IT to embed quality into contracts and transfers.

Qualifications

• 3+ years of GxP quality experience with direct vendor/CRO oversight or auditing.
• Knowledge of OECD GLP, 21 CFR Part 58, and ALCOA+ data integrity.
• Strong communication and negotiation skills.

Responsibilities

• Oversee external partners in nonclinical/GLP activities and ensure GLP/GCP/GMP compliance.
• Lead vendor lifecycle activities: due diligence, qualification, quality agreements, risk-based monitoring, CAPA.
• Develop and monitor KPIs, governance forums, and CAPA closure.
• Coordinate inspections readiness and support for audits.
• Embed quality requirements in scopes of work and contracts; train stakeholders.
• Maintain up-to-date knowledge of regulatory requirements and CSL standards.

Skills

Vendor oversight

Quality assurance

Regulatory knowledge

Auditing

Data integrity ALCOA+

GxP knowledge

Communication

Negotiation

Cross-functional collaboration

Education

Bachelor's degree in a relevant scientific discipline

Job description

GLP Vendor Oversight and QA Lead

The integrity of nonclinical data depends on more than what happens inside a company's walls. Much of the critical work in GLP-regulated research — safety studies, toxicology, analytical testing — is carried out by external laboratories and CROs. When that network of partners operates to the highest quality standards, the science is sound. When it doesn't, the consequences reach all the way to patients.

Why this role matters

GLP vendor oversight is often invisible when it's done well — and very visible when it isn't. As the internal authority on GLP and nonclinical vendor quality, you will be the person others turn to when the questions are difficult. If you take data integrity seriously, understand the regulatory landscape deeply, and want to shape how a global company manages its external nonclinical network, this is a role with real scope to make a difference.

About the role

Own quality oversight of external partners supporting nonclinical and GLP activities (CROs, laboratories, test facilities). Lead the vendor lifecycle: due diligence, qualification, quality agreements, risk-based monitoring, issue management and continuous improvement, ensuring adherence to GLP/GCP/GMP, data integrity and applicable regulations. Partner with Nonclinical Development, Procurement, Legal and IT.

• Vendor Lifecycle and Governance:Run risk-based qualification and requalification, draft and maintain Quality Agreements, and set vendor KPIs and governance forums, ensuring actions and CAPAs are closed.
• Inspections: Identify and prioritise vendors for audit on a risk basis; planning, conducting and grading sits with the audit function. Confirm vendor CAPAs are fit for purpose and run effectiveness checks. Coordinate inspection readiness and front- and back-room support.
• Quality Systems and Compliance:Ensure vendor practices meet GLP/GCP/GMP, OECD GLP, 21 CFR Part 58, ICH, ISO and data integrity (ALCOA+). Provide input on third-party deviations, change control, CAPA, and the QMS.
• Risk Management and Continuous Improvement:Lead vendor risk assessments (risk registers, FMEA) to set oversight frequency, improve vendor performance, and present trends at management reviews.
• Cross-Functional Partnership: Embed quality requirements in scopes of work and contracts, guide technology transfers and data flows, and train internal stakeholders.
• Maintain and share knowledge of Regulations and Requirements:Stay current with GLP and GxP regulations and translate changes into CSL requirements.

Position Qualifications and Experience Requirements:

Education:

Bachelor's degree in a relevant scientific discipline.

Experience

3+ years of GxP quality experience with direct vendor/CRO oversight and/or auditing (GLP/GCP/GMP), nonclinical/GLP preferred. Knowledge of OECD GLP, 21 CFR Part 58, Annex 11/Part 11 and data integrity (ALCOA+). Strong communication and negotiation skills.

Competencies

Works with limited supervision across multinational teams. Strong analytical, problem-solving, influencing and organisational skills. Knowledge of QMS implementation, regulatory frameworks and audit/inspection management.