Associate Director / Senior Manager, Quality Assurance (GCP Auditor)

TFS HealthScience; Italia; Ibrido; EUR 65.000 - 95.000; Tempo pieno

Descrizione del lavoro

A leading global Contract Research Organization is seeking an Associate Director / Senior Manager in Quality Assurance (GCP Auditor) for a hybrid role in Europe. The position involves conducting internal and external audits, managing audit findings, and ensuring compliance with regulatory standards. Applicants should have at least five years’ experience in clinical trials and possess a Life Science degree. This role offers competitive compensation and a collaborative work environment.

Servizi

Competitive compensation package

Comprehensive benefits

Opportunities for professional growth

Competenze

• Minimum five years' experience in clinical trials and quality assurance.
• Fluency in English, both written and verbal.
• Understanding of GCP/GxP regulations.

Mansioni

• Conduct internal and external GxP audits.
• Manage team during regulatory inspections.
• Support staff in preparing for client audits.

Conoscenze

GCP knowledge

Quality assurance

Analytical skills

Communication skills

Problem-solving abilities

Project management

Formazione

Life Science degree

Strumenti

MS Office

Descrizione del lavoro

Overview

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service (FSP) solutions.

Join Our Team as an Associate Director / Senior Manager, Quality Assurance (GCP Auditor) - hybrid in Warsaw, Poland or home based in Sweden, Italy or Portugal.

Responsibilities

• Prepares, conducts and follows up on all types of internal and external GxP audits
• Supports and provides leadership in clinical audit activities for both internal and external parties to ensure alignment with TFS standards, regulatory requirements, and quality expectations
• Works closely with Business Leads to coordinate appropriate and complete resolution of audit findings / non-compliant issues, quality investigations, etc. in a timely manner, including approval of corrective action and preventive action (CAPA) plans as required
• Conducts peer review of audit reports
• Supports and guides operational staff in preparing for customer audits
• Hosts client audits
• Prepares investigational sites for regulatory inspections, as required
• Guides operational staff in preparing for inspections including analysing risks and developing inspection readiness strategy
• Acts as a subject matter expert for inspectors and ensuring the Business Unit team members are fully prepared for interactions; provides training / preparation to the backroom support team
• Manages team during inspections
• Hosts and manages regulatory inspections for clients, as required

Quality Management System

• Facilitates teams from across the company in generating / updating Controlled Documents; driving the process to ensure Controlled Documents are aligned with the regulatory requirements and the applicable standards
• Supports staff from across the company to complete accurate and detailed risk assessments and root cause analysis for all Quality Issues, ensure they are completed on time and documentation is always suitable to share with clients as appropriate
• Assists staff to prepare appropriate and robust CAPA Plans (for Quality Issues), track and manage these through to completion ensuring the CAPAs are completed on the due date
• Drive and actively contribute to continuous improvement of the organisation and development of routines that aim to increase quality and improve compliance

Client Interactions

• Assists with business development of external quality and compliance services
• Leads / attends client visits / client meetings when required

Support

• Provide quality advice and support to internal clients and external clients
• Leads clinical non-compliance event investigations and CAPA implementation that may include monitoring non-compliance trends and effectiveness checks
• Identifies potential systemic gaps and coordinates with the appropriate stakeholders to ensure timely remediation. As appropriate, escalates issues of critical non-compliance and / or lack of urgency in remediation to the Head of Quality and Compliance

Qualifications

• University / college degree in a scientific area (Italy : Life Science degree level education is required)
• Awareness of the clinical trial area in the CRO and / pharma industry, including knowledge of GCP / GxP regulations
• Deep understanding of GCP / GxP regulations and standards to facilitate the interpretation and impact of findings of internal and external audits
• At least five (5) years’ experience in clinical trials, including quality assurance and quality operation experience. CSV knowledge and experience are a plus
• Adheres to ethical and good clinical practices and the ability to work as part of a team, as well as work independently in a remote workforce environment
• Excellent interpersonal and communication skills and the ability to work on multiple projects with competitive timelines
• Highly analytical professional with strong attention to detail and respect for the need for accuracy of information
• Pro-active, recognizing and anticipating issues, addressing problems and developing solutions
• Good planning, organisation and problem-solving abilities
• Demonstrated ability to multitask, prioritize, and complete objectives
• Excellent oral and written communication skills
• Fluent in English, both written and verbal
• Advanced user of MS Office applications (Outlook, Word, Excel, PowerPoint)

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

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