Quality Control Analytical Expert

Job Title: Quality Control Analytical ExpertLocation: Waterford, IrelandWorking Arrangement: Hybrid - 3 Days On-Site, 2 Days Working From Home RemotelyJob type: Full-Time, 12-Month Fixed Term ContractAbout the jobAs a Quality Control Analytical Expert, you'll provide analytical expertise to support method validation, transfers, troubleshooting, and investigations, while ensuring compliance with cGMP, quality, and safety standards. You'll work closely with cross-functional teams to drive analytical excellence and support continuous improvement across QC operations.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:Providing his/her analytical expertise for any project, troubleshooting, investigation on analytical methods and lab technologiesCoordinate analytical testing on projects (validation/transfer), ensuring adherence to the committed scheduled plansPerforming his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasksRecording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and data integrity requirementsWriting/reviewing protocols and reports related to analytical validation/transfers and qualification activitiesWriting/reviewing and maintaining accurate analytical methods proceduresInforming his/her manager of any quality or HSE event (deviations, OOx,...) in a

timely manner to ensure investigation and impact assessment are performed appropriatelyParticipating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriatelyPerforming periodically trend analysis on method performance to determine the need to revalidate, optimize, or replace the methodEnsuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriatelySupporting QC teams during internal and external audits and inspectionsAbout youSignificant 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.