Senior Technology Quality Auditor

TN United Kingdom; Uxbridge; On-site; GBP 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a Senior Technology Quality Auditor to enhance compliance and quality in clinical trials. This role involves conducting thorough audits, mentoring future auditors, and ensuring adherence to GxP regulations. The ideal candidate will possess a strong background in regulatory compliance and quality assurance, along with excellent analytical and problem-solving skills. Join a dynamic team dedicated to fostering a culture of continuous improvement and quality excellence. If you're ready to make a significant impact in a collaborative environment, this opportunity is for you.

Qualifications

• 5+ years in regulatory or clinical research, with 2+ years in quality assurance.
• In-depth knowledge of GxP regulations and auditing practices.

Responsibilities

• Lead audits across clinical research phases and ensure compliance.
• Train and mentor junior auditors while maintaining QA systems.

Skills

Regulatory Compliance

Quality Assurance

GxP Auditing

Analytical Skills

Problem-Solving Skills

Communication Skills

Education

Degree in Relevant Science

Master's Degree (Preferred)

Job description

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Senior Technology Quality Auditor, Uxbridge

Client: Parexel

Location: Uxbridge, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 59e81e538a2e

Job Views: 4

Posted: 02.05.2025

Expiry Date: 16.06.2025

Job Description:

When our values align, there's no limit to what we can achieve.

Technology Auditors possess significant authority within clinical trials, assessing technology, data integrity, and regulatory compliance. They recommend changes, provide guidance, and address compliance issues with stakeholders, impacting a culture of quality and continuous improvement.

The Senior Technology Auditor conducts audits affecting business operations, processes, and systems, ensuring high compliance standards. They possess in-depth knowledge of GxP regulations, Parexel procedures, and processes, and independently manage audits while mentoring others. They contribute to process improvements and ensure effective global and regional audit programs.

Responsibilities include leading and performing various audits across clinical research phases, reviewing responses to audit findings, and ensuring timely and quality reporting. They travel internationally as needed, support CAPA implementation, develop audit tools, and maintain QA systems. They also train and mentor less experienced auditors, ensuring adherence to procedures and fostering a collaborative environment.

Qualifications include at least 5 years of experience in regulatory or clinical research areas, with a minimum of 2 years in quality assurance and GxP auditing. A degree in a relevant science or technology field is required, with a master's degree preferred. Excellent communication, organizational, analytical, and problem-solving skills are essential, along with the ability to work effectively in multicultural and matrix environments.