Quality Control System Supervisor

Sanofi; Waterford; Hybrid; EUR 55,000 - 73,000; Full time

Job summary

Sanofi Waterford seeks a Quality Control System Supervisor to oversee quality processes and QC digital solutions, ensuring compliance with global processes and regulatory requirements. The role supports document control, data management, and end-user training across QC labs in a hybrid work arrangement.

You will drive continuous improvement in QC methods, support regulatory inspections, and represent QC in global communities. A degree in science or related field and GMP experience are expected.

Qualifications

• Experience in quality control within pharmaceutical industry, GMP & regulatory requirements.
• Strong analytical skills to interpret data and drive improvements.
• Attention to detail to ensure accuracy in testing and reporting.
• Ability to identify issues and implement effective solutions.

Responsibilities

• Oversee quality processes and QC digital solutions in line with Sanofi global processes.
• Issue and approve local QC documentation to support processes and tool usage.
• Maintain local QC procedures and templates per regulatory requirements.
• Implement and maintain QC digital solutions, including data management and end-user support.
• Archive QC documentation per global and regulatory requirements.
• Train and support end-users on QC processes and tools.
• Investigate QC events and resolve discrepancies within perimeter.
• Lead remediation actions from findings and CAPAs.
• Support regulatory inspections by presenting QC processes and records.
• Drive continuous improvement in QC processes and tool usage with QC excellence team.
• Represent QC in CoPs led by global; contribute to CoEs if requested.

Job description

Job details

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. Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

• The salary range for this position is :€54 800,00 - €73 067


• Employees may be eligible to participate in Company employee benefit programs.

We are an R&D driven, AI‑powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world. Discover more about us visiting www.sanofi.com or via our movie. We are Sanofi Start a career that makes a difference. Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug‑discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives.