Assurance Auditor

Description:

CPL & TAYLOR by Synergos srl, an established international consultancy specializing in Life Sciences regulatory and digital solutions, is seeking an experienced GCP/GVP Auditor to join their UK operations. Founded in 2010 and headquartered in Italy, the company partners with leading pharmaceutical and biotech firms, providing expert services across regulatory affairs, pharmacovigilance, clinical trials, quality assurance, and digital compliance solutions.

This is a key role within the Quality Assurance division, designed for professionals with strong knowledge of Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP) standards. You will manage audits, ensure regulatory compliance, and support clients in achieving audit readiness and continuous quality improvement. The position offers flexibility to work remotely or in a hybrid capacity, with some travel to client sites as needed.

Key Responsibilities:

• Conduct GCP/GVP audits for clients in the Life Sciences industry and prepare comprehensive audit reports.

• Collaborate with the QA Director to coordinate external auditors and ensure audit consistency.

• Develop, review, and update Standard Operating Procedures (SOPs) in line with current regulatory guidelines.

• Oversee day-to-day QA activities, ensuring delivery of high-quality services to clients.

• Monitor and report key compliance KPIs, identifying potential areas for improvement.

• Provide training and guidance on quality and regulatory compliance topics to internal teams and clients.

Required Skills and Qualifications:

• Minimum 5 years of experience as a GVP/GCP Auditor or Consultant in the Life Sciences field.

• Degree in scientific disciplines such as Pharmacy, Biology, Chemistry, or related fields.

• Proven expertise in GVP and GCP regulations and auditor qualification standards.

• Familiarity with the 2011 Legislative Decree on CROs and European regulatory frameworks.

• Ability to work independently in international and cross-functional environments.

• Willingness to travel domestically and internationally as required.

• Knowledge of Computer System Validation (CSV) will be considered an advantage.

What the Company Offers:

• Permanent full-time employment contract with competitive compensation.

• Gross annual salary around £60,000, based on experience and qualifications.

• Flexible working arrangements – remote or hybrid options available.

• A collaborative, inclusive, and multicultural work environment.

• Opportunities for career growth and participation in high-impact global projects.

• Access to continuous professional development and training programs.