Global GCP/PV Auditor (Remote)

Novartis

Barcelona

Presencial

EUR 45.000 - 84.000

Jornada completa

Hace 9 días
Generador de candidaturas

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Ventajas ofrecidas por este puesto de trabajo

Relocation support
Remote work options

Descripción de la vacante

Novartis is seeking a Global GCP/PV Auditor to ensure clinical and pharmacovigilance activities meet regulatory and internal standards. You will plan, lead and report audits across global operations, providing guidance and training to teams.

The role requires travel up to 50% and offers relocation support with the option to work remotely in Spain, with preference for Madrid or Barcelona area. You will contribute to continuous quality improvement and CAPA processes.

Formación

  • Degree in natural or biological sciences, or equivalent.
  • Approximately 5 years of experience in GCP, GPvP, clinical research, pharmaceutical industry or equivalent.
  • 1–2 years of GCP auditing experience preferred.
  • Strong knowledge of GCP, GPvP and GxP regulations.
  • Ability to manage multiple priorities and maintain oversight across parallel activities.
  • Fluent English; additional languages are an advantage.

Responsabilidades

  • Plan, lead, conduct, document, report and follow up on GCP/PV audits in accordance with Novartis procedures.
  • Perform low-risk GCP/PV audits, such as investigator site audits and vendor audits.
  • Support more complex audits including country organizations and higher-risk vendors.
  • Provide technical guidance and training on audit-related activities.
  • Escalate critical audit findings and support follow-up actions.
  • Ensure definition, documentation and follow-up of mitigation plans.
  • Assess adequacy of responses and CAPA plans with CAPA teams.
  • Maintain up-to-date knowledge of regulations, standards and guidelines.

Conocimientos

GCP auditing
GPvP auditing
GxP regulations
Quality compliance
Stakeholder engagement
Leadership
English proficiency

Educación

Biological sciences degree

Descripción del empleo

Novartis is seeking a Global GCP/PV Auditor to ensure clinical and pharmacovigilance activities meet regulatory and internal standards. You will plan, lead and report audits across global operations, providing guidance and training to teams.

The role requires travel up to 50% and offers relocation support with the option to work remotely in Spain, with preference for Madrid or Barcelona area. You will contribute to continuous quality improvement and CAPA processes.

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