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Manufacturing and Supply

Manufacturing and Supply
Where the
miracles of
science
are made
a reality
for patients

QC Analyst (Data Reviewer)

Waterford, Ireland Salary Range   EUR 48,000.00 - 64,000.00
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At a glance

Our teams produce and deliver over 4 billion units of medicines and vaccines every year, ensuring every breakthrough gets to the people who need it most.
Our state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation are redefining what’s possible: ensuring treatments reach patients faster, safer, and more sustainably than ever before. This is where your skills, ambition, and passion can shape the future of healthcare.

Job Title: QC Analyst (Data Reviewer)

FTC - 23 month fixed term contract


Our Team 

Quality Control (QC) is responsible for sample receipt, testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation. 

The Quality Control Operations group supports Laboratory Investigations, Deviation Investigations, CAPA support, Training, and Change Controls. Quality Control Validation Support consists of the Method Validation Group and the Equipment Qualification Group. Quality Control is also responsible for assisting in site-wide studies and projects. 

Main Responsibilities:

• Executing analytical testing in a timely manner, ensuring adherence to the committed

scheduled plans

• Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks

• Recording all expected raw data, calculations, information, related to his/her tasks, to

comply with cGMP and data integrity requirements

• Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified

• Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plan

• Informing his/her manager of any quality or HSE event (deviations, OOx,…) in a timely manner to ensure investigation and impact assessment are performed appropriately

• Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately

• Executing assigned CAPAs related to remediation plans, continuous improvements

• Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately.

• Perform data review in a timely manner, ensuring adherence to committed scheduled plans 

• Perform tasks in accordance with cGMP and HSE requirements, following all associated instructions, procedures, and records 

• Verify all expected raw data, calculations, and information to comply with cGMP and data integrity requirements 

• Ensure appropriate training and qualification for assigned methods 

• Inform management of any quality or HSE events (deviations, out-of-specification results) promptly to ensure proper investigation and impact assessment 

• Support investigations to ensure thorough analysis and appropriate impact assessment 

• Maintain laboratory facilities and instruments in quality and safety status to ensure appropriate use 

About you 

Education: BSc in Chemistry, Biochemistry, or a related science discipline 

Experience: Background in an analytical chemistry laboratory environment 

•Experience with cGMP and laboratory safety requirements 

• Analytical testing and data review capabilities 

• In depth understanding of data integrity principles and good documentation practices 

• Experience with Biologics and/or HPLC/UPLC, CE, KF, HIAC, ELISA, FTIR

•Excellent attention to detail and accuracy in documentation 

• Strong communication skills for reporting and collaboration 

• Problem-solving abilities for investigations 

• Commitment to quality and safety standards 

• Team collaboration and active participation  

• Demonstrated ability to prioritise tasks and adhere to agreed timelines 

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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, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. 

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! 

Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.

Apply now
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Why work with us

  • We’re problem-solvers and pioneers. United by the belief that everyone deserves a healthier future. We create best-in-class vaccines that prevent disease and protect lives.

  • Innovation drives us. From AI and mRNA to next-gen science, we push the boundaries to deliver first- and best-in-class vaccines for infectious diseases worldwide.

  • Growth happens here. With bold investments in R&D and world-class facilities, Sanofians across the entire vaccine lifecycle are shaping the future of global health.

  • We do what’s right. Sustainability and DE&I drive our positive global impact—because the diverse communities Sanofians represent are the patients we serve.

All-in on diversity

At Sanofi, diverse perspectives fuel the best solutions for patients. Hear from Monique Vessey, our Supply Chain Transformation Leader, on how her background shapes her approach to delivering life-changing medicines.

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