Fabrication et Approvisionnement
Là où les miracles
de la science
deviennent une réalité pour les patients

Job title: Quality Control System Supervisor

• Location: Waterford, Ireland
• Working Arrangement: Hybrid - 3 Days On-Site, 2 Days Working From Home Remotely
• Job type: Full-Time, 12-Month Fixed Term Contract

About the job

The Quality Control system team will have responsibility to oversee all quality processes and digital solutions related to quality control management and to ensure compliance with the Sanofi global processes. The team also supports the delivery of ongoing QC continuous improvement initiatives.

Ready to get started?

Main responsibilities:

• Overseeing all quality processes and digital solutions related to quality control management in compliance with the Sanofi global processes and quality control tools

• Ensuring issuance and approval of all appropriate local quality control documentation, such as local procedures, templates… to support the QC processes and QC digital system usage, in the QC labs, in accordance with the Sanofi global processes.

• Ensuring quality control processes supported by appropriate procedures are implemented locally and maintained, in line with Sanofi global and regulatory requirements.

• Ensuring implementation and maintenance of QC digital solution (core model and local) (including data management and end-user management)

• Ensuring archiving of all QC documentation, in compliance with the Sanofi global requirements and regulatory.

• Ensuring training and support of end-users on QC processes and tools, in coordination with Sanofi global teams

• Investigating on a timely manner and resolving any quality control events, issues or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs.

• Providing support during regulatory inspections and audits by presenting QC processes and QC digital solution documents and records

• Leading initiatives for continuous improvement in QC processes and tools usage, in coordination with QC excellence team.

• Being representative of the site in the related CoPs led by the global, for the process in his/her scope, and if requested participating in the CoEs, and ensuring local communication.

• Being representative of QC for the processes led by QMS team at site level

About you

• Demonstrable experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements.

• Third level qualification (degree in science or related discipline) or appropriate relevant experience supplementing lower grade scientific qualification.

• Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement.

• Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.

• Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.

Why choose us?

Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.