Gcp / Gvp Auditor
Posted Today by CPL & TAYLOR by Synergos srl
£60,000 Per year
Undetermined
Hybrid
Greater London, England, United Kingdom
Summary: The GCP/GVP Auditor role at CPL & TAYLOR By Synergos involves managing Quality Assurance projects within the Life Sciences sector, ensuring audit readiness and regulatory compliance. The position offers flexible working arrangements, including full remote or hybrid options, and requires significant experience in GVP/GCP auditing. The successful candidate will conduct audits, develop SOPs, and deliver training on quality and regulatory topics. This permanent, full-time position is based in Greater London, England, with a gross annual salary of around £60,000.
Key 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
Key Skills:
- 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
Salary (Rate): £60,000 yearly
City: Greater London
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Consulting
CPL & TAYLOR By Synergos, Is Looking For GCP / GVP AUDITOR (Rif. ANN411296)
LOCATION: UK – possibility of full remote or hybrid work, with travel required
CONTRACT: Permanent, full-time
SALARY: Gross annual package around £60.000
The 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.
The 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
The 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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CPL & Taylor By Synergos Srl Ricerca e Selezione del Personale – Aut. MLSPS Prot.13/I/0008775 Mantova – Parma – Verona – Modena – Brescia – Cremona Main Office: +39 0376 324703 #StepUpWithSynergos