GCP / GVP AUDITOR

CPL & Taylor by Synergos Srl; Italia; Ibrido; EUR 69.000; Tempo pieno

Descrizione del lavoro

A leading consulting firm is seeking a GCP/GVP Auditor to manage Quality Assurance projects in the Life Sciences sector. The role involves conducting audits, coordinating with auditors, and ensuring regulatory compliance. Candidates should have at least 5 years of experience, a degree in scientific disciplines, and strong knowledge of GVP/GCP regulations. Competitive salary of £60,000 with flexible work options will be provided.

Servizi

Flexible working arrangements

Career growth opportunities

Continuous professional training

Competenze

• At least 5 years of experience as a GVP/GCP Auditor or Consultant.
• Familiarity with the 2011 Legislative Decree on CROs is beneficial.
• Experience in international environments and willingness to travel.

Mansioni

• Conduct GCP/GVP audits at client sites and prepare related reports.
• Coordinate external auditors in collaboration with the QA Director.
• Develop and review SOPs to ensure compliance with regulatory requirements.

Conoscenze

GVP/GCP regulations knowledge

Audit management

Training delivery

Compliance monitoring

Formazione

Degree in scientific disciplines

Strumenti

Computer System Validation

Descrizione del lavoro

Company

An important international organization specializing in consulting and digital solutions for the Life Sciences sector, with headquarters in Italy. Established in 2010, it supports pharmaceutical and biotech companies in regulatory affairs, pharmacovigilance, clinical trials, medical affairs, and quality assurance. The company provides innovative digital tools and high value-added services, with a strong focus on regulatory compliance and operational efficiency.

Location, Contract and Salary

Location: UK – possibility of full remote or hybrid work, with travel required. Contract: Permanent, full-time. Salary: Gross annual package around £60,000.

Role

As a GCP/GVP Auditor, you will be involved in managing Quality Assurance projects for clients operating in the Life Sciences industry. The goal is to ensure audit readiness, regulatory compliance, and continuous improvement of QA processes.

Main Responsibilities

• Conduct GCP/GVP audits at client sites and prepare related reports
• Coordinate external auditors in collaboration with the QA Director
• Develop and review SOPs to ensure compliance with regulatory requirements
• Supervise daily activities related to the provision of QA services
• Monitor key compliance KPIs
• Deliver training on quality and regulatory topics

Requirements

• At least 5 years of experience as a GVP/GCP Auditor or Consultant
• Degree in scientific disciplines
• Strong knowledge of GVP/GCP regulations and auditor qualification
• Familiarity with the 2011 Legislative Decree on CROs
• Experience in international environments and willingness to travel
• Knowledge of Computer System Validation is considered a plus

Company Offers

• Full-time, permanent employment contract
• Gross annual salary around £60,000, depending on experience
• Flexible working arrangements (remote or hybrid options)
• Inclusion in a collaborative and multicultural team
• Career growth opportunities and high-impact projects
• Continuous professional training

All job postings are open to applicants of all genders (L.903/77).

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