Executive Director, D&T Quality Validation and Process in Uxbridge
Executive Director, D&T Quality Validation and Process

Executive Director, D&T Quality Validation and Process in Uxbridge

Uxbridge Full-Time 72000 - 108000 ÂŁ / year (est.) Home office possible
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At a Glance

  • Tasks: Lead a global team to enhance technology quality and compliance in biopharmaceutical services.
  • Company: Join Parexel, a leader in transforming scientific discoveries into new treatments.
  • Benefits: Enjoy competitive salary, bonuses, company car, and comprehensive benefits.
  • Why this job: Make a real impact on global health while developing your career in a supportive environment.
  • Qualifications: Experience in GxP system validation and strong leadership skills required.
  • Other info: Flexible remote work options available across the UK, Poland, or Romania.

The predicted salary is between 72000 - 108000 ÂŁ per year.

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.

This role will work within our innovative Data & Technology group that continues to evolve to meet business needs, fuel Parexel's growth and enable improved support for stakeholders, including customers and ultimately patients, who will benefit from Parexel's integrated processes and systems. This role can be based in the UK, Poland or Romania and can be fully home based.

This position will involve enhancing and developing an innovative, collaborative environment by leading an international team, partnering with senior peers, and working closely with an engaged senior leader.

As the Executive Director, Systems Quality, Validation & Processes you will be the senior leader responsible for establishing and overseeing Parexel’s global technology quality lifecycle, computerized system validation (CSV), and process governance across all Data & Technology (D&T) solutions. You will ensure that all systems—particularly those impacting clinical development, safety, regulatory, and enterprise operations—adhere to GxP expectations, global regulatory standards, and internal quality frameworks.

You will provide enterprise-level leadership to ensure “audit ready” consistent system validation practices, optimized processes, and strong collaboration between technology, business, quality, and compliance stakeholders.

Key Responsibilities & What You’ll Do
  • Systems Quality & Compliance Leadership
    • Define and lead the enterprise-wide technology quality strategy, ensuring alignment with GxP expectations, ICH, EMA, FDA, and internal quality policies.
    • Govern compliance with the Technology SOPs.
    • Ensure systems remain in a validated and audit-ready state throughout their lifecycle, including upgrades, changes, integrations, and decommissioning.
  • Computerized System Validation (CSV) Governance & Oversight
    • Oversee lifecycle validation activities for all D&T systems, enabling a risk-based, scalable, automated validation program.
    • Lead the enterprise validation framework—including planning, risk assessments, requirements, testing, traceability, reporting, and periodic review.
    • Govern validation team roles (System Owner, Business Analyst, Technology Representative, Validation Representative, Quality Representative, SME).
    • Drive standardization of validation documentation, templates, and tools across all technology domains.
  • Process Optimization, Standards & Governance
    • Lead the definition, deployment, and continuous improvement of technology delivery processes (SDLC, change management, testing, documentation, release management).
    • Ensure cross-functional alignment between D&T, Quality, Compliance, Clinical Operations, Safety, and Regulatory.
    • Serve as the executive owner of validation policy updates and procedural improvements.
  • Test Strategy, Execution, Quality Engineering & Tooling Enablement
    • Oversee and execute functional, automated, regression, integration, smoke, and user acceptance testing activities.
    • Promote continual improvement and automation capabilities that reduce validation burden while improving consistency and traceability.
    • Establish enterprise standards for test evidence, defect management, and quality metrics.
  • Vendor, System, and Risk Management
    • Govern the process for reviewing vendor validation packages, reliance strategies, and partner oversight.
    • Ensure all third-party systems meet Parexel’s quality and validation expectations.
    • Lead risk-based decision-making frameworks for validation effort, documentation rigor, and mitigation plans.
  • Cross-Functional Partnership & Strategic Alignment
    • Collaborate with D&T and business executive leadership, Data Governance to ensure cross-functional integration of quality and validation standards.
    • Ensure alignment with broader D&T organizational strategies and roadmaps.
    • Partner closely with Clinical, Safety, Regulatory, and Operational groups to ensure their systems maintain compliance during rapid change.
    • Lead a global team across system quality assurance, validation engineering, process governance, and compliance.
    • Establish competency frameworks aligned with skills in D&T Quality & Validation functions.
    • Promote a culture of accountability, precision, continuous improvement, and proactivity in compliance.
Education
  • Bachelor’s degree in Computer Science, Engineering, Life Sciences, Quality Engineering, or related field required.
  • Master’s degree or equivalent experience preferred.
Skills
  • Deep expertise in GxP system validation, computerized system lifecycle management, and global regulatory requirements.
  • Strong understanding of testing methodologies, validation frameworks, and risk-based quality approaches.
  • Exceptional leadership skills with ability to influence across technology, quality, and business groups.
  • Highly skilled in process design, optimization, SDLC governance, and audit readiness.
  • Strong analytical, documentation, and problem-solving capabilities.
Knowledge And Experience
  • Very strong Senior Director or Executive Director level experience in technology quality assurance, software validation, regulatory compliance, or related disciplines.
  • Proven experience leading global quality and validation programs across complex system landscapes.
  • Deep familiarity with validation documentation standards and roles.
  • Experience with test management tools, automated testing platforms, and enterprise quality systems.
  • Experience supporting clinical, safety, regulatory, or GxP-relevant enterprise systems strongly preferred.

In return we will be able to offer you a structured career pathway and encouragement to develop within the role including awareness and understanding of the industry. You will be well supported and in return for your hard work you will be rewarded with a competitive base salary, bonus, company car or car allowance, holiday as well as other leading benefits you would expect with a top company in the CRO Industry.

Apply today to begin your Parexel journey!

Executive Director, D&T Quality Validation and Process in Uxbridge employer: Parexel

At Parexel, we are dedicated to improving global health through innovative biopharmaceutical services, and as an Executive Director in our Data & Technology group, you will thrive in a collaborative and empowering environment. With the flexibility of remote work from the UK, Poland, or Romania, we offer a structured career pathway, competitive salary, and comprehensive benefits, ensuring that your contributions are recognised and rewarded while you lead a talented international team committed to excellence in quality and compliance.
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Contact Detail:

Parexel Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Executive Director, D&T Quality Validation and Process in Uxbridge

✨Tip Number 1

Network like a pro! Reach out to connections in the industry, attend relevant events, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!

✨Tip Number 2

Prepare for those interviews by researching Parexel’s values and recent projects. Show us that you’re not just another candidate; demonstrate how your experience aligns with our mission of improving health and supporting patients.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. We want to see you shine when discussing your leadership skills and expertise in quality validation.

✨Tip Number 4

Don’t forget to follow up after your interview! A simple thank-you email can go a long way in showing your enthusiasm for the role. Plus, it keeps you fresh in our minds as we make our decisions.

We think you need these skills to ace Executive Director, D&T Quality Validation and Process in Uxbridge

GxP System Validation
Computerized System Lifecycle Management
Global Regulatory Requirements
Testing Methodologies
Validation Frameworks
Risk-Based Quality Approaches
Leadership Skills
Process Design
SDLC Governance
Audit Readiness
Analytical Skills
Documentation Skills
Problem-Solving Skills
Test Management Tools
Automated Testing Platforms

Some tips for your application 🫡

Tailor Your Application: Make sure to customise your CV and cover letter to highlight how your experience aligns with the role. Use keywords from the job description to show that you understand what we're looking for.

Showcase Your Leadership Skills: As an Executive Director, we want to see your leadership style shine through. Share specific examples of how you've led teams or projects in the past, especially in areas related to quality and compliance.

Be Clear and Concise: Keep your application straightforward and to the point. We appreciate clarity, so avoid jargon and ensure your key achievements are easy to spot. This helps us quickly see why you're a great fit!

Apply Through Our Website: Don't forget to submit your application through our official website! This ensures it gets to the right people and helps us keep track of all applications efficiently.

How to prepare for a job interview at Parexel

✨Know Your GxP Inside Out

Make sure you have a solid understanding of GxP regulations and how they apply to technology quality and validation. Brush up on the latest guidelines from ICH, EMA, and FDA, as these will likely come up during your interview.

✨Showcase Your Leadership Skills

Prepare examples that highlight your leadership experience, especially in managing global teams and cross-functional partnerships. Be ready to discuss how you've influenced change and driven process improvements in previous roles.

✨Demonstrate Your Problem-Solving Abilities

Think of specific challenges you've faced in technology quality assurance or validation and how you overcame them. This role requires strong analytical skills, so be prepared to showcase your problem-solving capabilities with real-life examples.

✨Align with Parexel's Values

Familiarise yourself with Parexel's core values: Patients First, Quality, Respect, Empowerment, and Accountability. Be ready to discuss how these values resonate with you and how you can embody them in your role as Executive Director.

Executive Director, D&T Quality Validation and Process in Uxbridge
Parexel
Location: Uxbridge

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  • Executive Director, D&T Quality Validation and Process in Uxbridge

    Uxbridge
    Full-Time
    72000 - 108000 ÂŁ / year (est.)
  • P

    Parexel

    5000+
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