Corporate Quality Auditing Senior Specialist

Questa posizione è in Chiesi Group
Riassunto dell'opportunità da parte della   Joinrs AI   :
Chiesi Group   cerca un   Corporate Quality Auditing Senior Specialist   con laurea in discipline scientifiche come Farmacia, Chimica o Biologia. Il candidato sarà responsabile della conduzione autonoma di audit GMP/ISO, della qualificazione e del monitoraggio dei fornitori globali secondo gli standard di qualità Chiesi. L’offerta include un contratto a tempo indeterminato presso Parma, con benefit competitivi, formazione continua e possibilità di lavoro flessibile.

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- Il processo di selezione sarà interamente gestito da Chiesi Group.
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- Corporate Quality Auditing Senior Specialist
Date: 9 May 2026
Department:
Corporate Quality Operations
Business Area:
Quality
Job Type: Direct Employee
Contract Type:
Permanent

Location:

Parma, IT

About us
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas.
At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.
Diversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.
Global Technical Operations & Supply
Global Technical Operations & Supply (Global Tech Op&S) is Chiesi’s global manufacturing and supply area, responsible for ensuring consistent, outstanding quality, service and value across our end‑to‑end supply chain. Global Tech Op&S oversees the entire lifecycle of the drug: from process optimization and industrialization, to manufacturing, engineering, quality oversight, and supply chain management. Throughout this journey, Operational Excellence drives continuous improvement.

This end‑to‑end model is powered by our four manufacturing sites - Parma (IT), Blois (FR), Santana de Parnaíba (BR), and Nerviano (IT) - together with our Virtual Plant network of external partners.
Who we are looking for
This is what you will do
Carry out GMP/ISO audits of GMD contractors in full autonomy
Draft quality agreements
Ensure supplier qualification and validation according to GxP requirements and Chiesi quality standards
Ensure the quality of global suppliers and monitor their quality performance
You will be responsible for
Within the scope of Good Manufacturing Practices (GMP), Good distribution practices (GDP) and ISO 9001:2015 standards:
Collaborate in internal/external audit activities at every stage:
Planning and updates
Issue annual audit plans (internal/external)
Preparation (material collection, procedures, official documentation)
Draft Audit agenda
Contact suppliers to be inspected
Conduct audits in Europe and worldwide
Draft audit reports in English
Check proposed corrective actions
Monitor progress and closure of corrective actions
Verify effectiveness of corrective actions
Prepare synoptic tables on audit status for management review

Participate in drafting and maintaining sector operating procedures, including:
Procedures for GxP suppliers and service providers qualification, validation, maintenance, quality risk management, instructions, templates, user guides
Procedures related to GxP audits
Review supply chain map, quality agreements

Investigate non-conformities of materials in acceptance, collaborating with internal representatives and global suppliers to promote corrective actions
Evaluate change controls related to suppliers, CMO, GxP service providers:
Assess impacts on qualification, audits, quality agreements, validations, supporting documents
Sup…