QC Analyst (Data Reviewer)

Sanofi Group; Waterford; On-site; EUR 48,000 - 64,000; Full time

Job summary

Sanofi is seeking a QC Analyst (Data Reviewer) for a 23-month fixed term contract at our Ireland site in Waterford. You will execute analytical testing, review data, ensure cGMP compliance and maintain data integrity across all tasks.

The role requires a BSc in Chemistry or related field, hands-on experience in an analytical lab, and strong collaboration across QA, QC and investigations. You will contribute to CAPAs, method qualification and ongoing lab improvements while adhering to safety

Qualifications

• BSc in Chemistry, Biochemistry, or a related science discipline.
• Experience in analytical chemistry lab and cGMP environment.
• Strong data integrity and good documentation practices.

Responsibilities

• Execute analytical testing in a timely manner per scheduled plans.
• Record all raw data, calculations and information to ensure data integrity.
• Perform QC data review of tests conducted by other analysts.
• Ensure training and qualification for assigned analytical methods.
• Support investigations and CAPAs as needed.
• Maintain lab facilities and instruments in quality and safety status.
• Inform management of quality or HSE events promptly.

Skills

Analytical testing

Data review

GMP compliance

Documentation

Investigations

Attention to detail

Communication

Time management

Education

BSc in Chemistry/Biochemistry or related science

Tools

HPLC/UPLC

ELISA

KF

HIAC

CE

FTIR

Job description

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

--- 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 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!

Salary & Benefits

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.

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.