Job title: QC Support Expert
Hiring Manager: Quality Control Manager
Location: Aventis Pharma Manufacturing, Jurong, Singapore
Transform Lives Through Excellence in Quality Control
At Sanofi, we deliver 4.3 billion healthcare solutions to people every year, transforming the practice of medicine through breakthrough science that improves people's lives. Our Manufacturing & Supply teams ensure this impact through flawless planning and meticulous attention to detail. With your expertise in Quality Control, you'll help us protect more people from infectious diseases and bring hope to patients and their families worldwide.
Your Impact
As our Quality Control Support Expert, you'll be the cornerstone of laboratory excellence, ensuring compliance, efficiency, and continuous improvement in our quality control operations. Your expertise will directly contribute to patient safety and product quality through:
Key Responsibilities:
Equipment & Systems Management
Ensure comprehensive lifecycle management of QC laboratory equipmentLead qualification and maintenance operations for QC equipmentEstablish metrics and monitor qualification activities to identify trendsEnsure all QC equipment are properly qualified and maintainedServe as SME for Labware LIMS and collaborate with global functionsTechnical Leadership & Method Management
Lead compendial compliance assessment and adherence for the QC laboratorySupport annual method reviews within the product review frameworkLead periodic analytical method control trend reviews and recommend improvementsSupport the invalid assay trending program in the QC laboratoryParticipate in Change Control Request facilitation for QC test methodsDigital & Data Management
Implement and maintain QC digital solutions (core and local models)Ensure proper documentation, review, and approval of qualification deliverablesRecord all required data and calculations in compliance with cGMP and Data Integrity requirementsProvide technical system administrator support for QC GXP computerized systemsQuality & Compliance
Maintain site validation master plan and procedures related to ALCM and CPVInvestigate and resolve quality control events promptlyProvide support during regulatory inspections and auditsRepresent the site in Communities of Practice (CoPs) led by global teamsDeputize as QC Manager when requiredSafety & Continuous Improvement
Ensure compliance with HSE policies and site proceduresEmbrace Zero Incident Mindset and adhere to Life Saving RulesLead initiatives for continuous improvement in QC support processesPractice and communicate laboratory safety standardsWhat You Bring
Strong chemistry background with technical expertise in laboratory equipment qualification and analytical method validationExperience with LIMS and laboratory computerized systemsKnowledge of cGMP, data integrity requirements, and regulatory standardsExcellent problem-solving skills and attention to detailStrong communication and collaboration abilitiesCommitment to quality, safety, and continuous improvementWhy Join Us?
Join our team and be part of a mission that matters. At Sanofi, you'll have the opportunity to grow professionally while making a meaningful difference in patients' lives. Your expertise in quality control will directly contribute to our ability to deliver safe, effective healthcare solutions globally.
Ready to get started? Apply now and help us chase the miracles of science to improve people's lives.
Pursue progress, discover extraordinaryBetter 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!