QC Analyst (Data Reviewer)

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

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.