Posted 27 August, 2026
Quality Control Analyst / Data Reviewer
Sanofi
Waterford, Waterford, Ireland
Full Time
Reference: 406242081
Quality Control Analyst (Data Reviewer)
Location: Waterford, Ireland
Job Type: 23-month FTC
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About the job
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
• 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
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About you
Education: BSc in Chemistry, Biochemistry, or a related science discipline
Experience: Background in an analytical chemistry laboratory environment
Technical skills:
• 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, ICE techniques
Soft skills:
• 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!
#LI-EUR
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.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
The salary range for this position is :€48 000,00 - €64 000
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.
Location: Waterford, Ireland
Job Type: 23-month FTC
---
About the job
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
• 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
Technical skills:
• 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, ICE techniques
Soft skills:
• 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
---
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!
#LI-EUR
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.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
The salary range for this position is :€48 000,00 - €64 000
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.
