Gcp/Pv Auditor

hace 4 días


Madrid, Madrid, España Novartis Farmacéutica A tiempo completo

Role Overview

As a Gcp/Pv Auditor, you will lead, support, and report independent Gcp/Pv audits and approve follow-up corrective and preventive activities according to Novartis Quality Systems and Standards. You will provide Gcp/Pv related quality guidance and assist in the identification and implementation of quality assurance training needs for Global GxP Audit and other business partners.

Responsibilities

  • Plan, lead, conduct, document, report, and follow-up of Gcp/Pv audits according to Novartis procedures and applicable regulations, standards, quality agreements, and guidance.
  • Provide technical guidance and training on audit activities.
  • Ensure appropriate escalation to responsible management in case of critical audit findings and support immediate follow-up measures.
  • Maintain current knowledge of regulations, standards, and guidance documents.

Requirements

  • Degree in natural/biological sciences or equivalent.
  • 5 years Gcp/Gpv/clinical/industry/health authority experience or equivalent.
  • Thorough knowledge of applicable Gcp, Gpv, and Gxp regulations, guidelines, policies, and procedures.

Why Novartis?

Our purpose is to reimagine medicine to improve and extend people's lives. With our people, we drive each day to reach our ambitions. Be part of this mission and join us.


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