QA GMP Senior Auditor

1 giorno fa

reggio emilia, emilia romagna, Italia Chiesi Tempo pieno
Overview

In this role you will support the execution of audits (second and first party), qualify R&D suppliers, and manage Quality Agreements to ensure GMP compliance for sterile, biological, and biotech products. You will collaborate with cross-functional teams and external consultants to drive quality assurance across supplier networks. The position offers hands-on audits, KPI data review, and SOP standardisation within a performance-driven, global R&D context. This is a chance to contribute to high-stakes compliance in gene therapies and advanced platforms.

Retribuzione / Benefits
  • annual bonus
  • pension
  • private medical insurance
  • wellbeing programme
  • flexible benefits programme
  • relocation support
Responsabilità
  • Plan and execute second party audits of GMP suppliers and GMP service providers (CMOs, contract laboratories)
  • Execute first party audits
  • Monitor corrective and preventive actions and ensure timely closure
  • Coordinate external consultants supporting Auditing & Supplier Qualification - GMP & Medical Device Unit
  • Define, review and finalise Quality Agreements with GMP suppliers and service providers
  • Support hosting of GMP inspections
  • Collect and review data for Management Review and KPIs/metrics
  • Finalize and standardise SOPs related to auditing and supplier qualification processes
  • Organise and support training on GMP requirements and related procedures
  • Act as QA reference for audit and qualification activities involving sterile, biological and biotech products
  • Interact with CMC, Regulatory Affairs, Clinical Supply, Procurement and cross-functional teams to qualify providers
Requisiti fondamentali
  • Scientific degree, preferably in Pharmacy, Chemistry, Biology, Biotechnology, Pharmaceutical Sciences or related discipline
  • At least three years of experience as auditor in pharmaceutical companies
  • Experience in Quality Assurance, supplier qualification or audit activities within pharmaceutical development or manufacturing
  • Knowledge of GMP requirements
  • Knowledge of auditing techniques
  • Knowledge of sterility assurance principles and GMP expectations for sterile and biotech products
  • Leadership
  • Organisational skills
  • Stress management
  • Knowledge of GMP requirements
  • Auditing techniques
  • Sterility assurance principles