Quality Control System Supervisor

Sanofi; Waterford; Hybrid; EUR 60,000 - 80,000; Full time

Job summary

Sanofi Waterford is seeking a Quality Control System Supervisor to oversee QC processes and digital solutions, ensuring compliance with global Sanofi standards. The role includes documentation control, local procedure support, training, and CAPA remediation.

You will contribute to continuous QC improvement, support regulatory inspections, and collaborate with global teams to ensure seamless quality management and data integrity in a hybrid work environment.

Qualifications

• Experience in quality control within the pharmaceutical industry.
• Third level qualification (degree in science or related discipline) or equivalent experience.
• Ability to analyze complex data and laboratory results for informed decisions.
• Keen attention to detail to ensure testing accuracy and regulatory compliance.
• Proven ability to identify issues and implement effective solutions.

Responsibilities

• Oversee quality processes and digital QC solutions in line with global Sanofi processes.
• Issue and approve local QC documentation to support QC processes and system usage.
• Ensure QC procedures are implemented locally and maintained per regulatory requirements.
• Manage QC digital solutions, data management and end-user support.
• Archive QC documentation per global and regulatory requirements.
• Train end-users on QC processes and tools in coordination with global teams.
• Investigate quality events and implement remediation actions and CAPAs.
• Support regulatory inspections by presenting QC processes and records.
• Lead continuous improvement initiatives in QC processes and tool usage.

Skills

Quality control

GMP knowledge

Data analysis

Regulatory compliance

Documentation

Education

Degree in science or related discipline

Tools

QMS software

QA software

Job description

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?

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

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?

• Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
• Transform lives worldwide by delivering life-changing treatments anywhere, anytime.
• Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.
• Help deliver 30+ new product launches by 2030, ensuring patients get treatments faster than ever.