Technology Quality Oversight Specialist - Parexel

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

TECHNOLOGY QUALITY OVERSIGHT SPECIALIST

About the Role

Join Parexel 's Technology Quality team to support quality oversight across our technology solution lifecycle. You'll provide validation expertise, risk assessment support, compliance monitoring, and inspection readiness for GxP and business-critical systems.

Partner with business stakeholders, Solution Validation Services, Digital and Technology, and Corporate Quality to ensure technology solutions remain compliant, fit for intended use, and inspection-ready throughout their lifecycle.

Key Responsibilities

• Provide quality oversight for technology solution development, validation, implementation, and maintenance.
• Independently review validation packages, including requirements, risk assessments, testing evidence, traceability, and validation reports to ensure compliance and inspection readiness.
• Monitor compliance with regulatory requirements, industry standards, and established procedures.
• Serve as a Quality Representative for technology quality issues, audit findings, CAPAs, and compliance initiatives, partnering with stakeholders to drive timely and effective resolution.
• Facilitate root cause analysis activities, remediation planning, and CAPA development to address technology-related compliance and validation issues.
• Assess AI-enabled solutions and emerging technologies for quality and compliance.
• Support customer audits, regulatory inspections, and internal audits by serving as a technology quality subject matter expert and facilitating responses to validation and compliance inquiries.
• Assist with supplier and vendor quality assessments.
• Maintain inspection-ready documentation and support audit readiness.

What We're Looking For

Required Experience

• 3–5 years in computerized system validation, technology quality, clinical research, pharmaceutical quality, or GxP-regulated environments

• Experience supporting technology projects and validation activities

• Knowledge of SDLC, validation lifecycle, change control, CAPA, and risk management

Key Skills

• Working knowledge of computerized system validation principles

• Understanding of GxP regulations (GCP, electronic records/signatures)