{"id":3530922,"url":"https://alion.io/job/sanofi-quality-control-pcu-manager-incoming-and-device","title":"Quality Control PCU manager (Incoming and Device)","company":{"id":146,"name":"Sanofi","domain":"sanofi.com","url":"https://alion.io/company/sanofi","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":92,"open_postings":76,"ghost_share":0,"stale_share":0.276,"repost_share":0.066,"time_to_fill_p50_days":22,"computed_at":"2026-11-03T05:54:40Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Waterford, Ireland"],"countries":["IE"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":57000,"max_usd":122000,"period":"year","method":"role_country_seniority_unknown","sample_n":124},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-10-30T16:00:58Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-03T14:37:08Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"Job Title: Quality Control PCU Manager (Incoming and Device)\nLocation: Waterford, Ireland\nJob Type: 12-Month FTC, Full-Time\nWorking Arrangements: On-site\nAbout the job\nQuality 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.\nReady to get started?\nJoin 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.\nAbout Sanofi\nWe’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.\nMain Responsibilities\nOverseeing daily operations of the quality control laboratory to ensure adherence to the committed scheduled plans\nMaintaining his/her laboratory in compliance with the GMPs and quality control processes defined according to internal and external quality requirements and regulations\nEnsuring the use of validated methods in his/her perimeter and executing any validation/transfer protocol as receiving unit\nManaging and training laboratory staff, ensuring they follow best practices and safety guidelines\nEnsuring his/her laboratory staff is qualified to perform the testing execution by maintaining the lab qualification matrix\nConducting routine shopfloor of laboratory to identify improvement opportunities\nEnsuring accurate and timely testing of received samples according to his/her perimeter\nReviewing and approving laboratory test results and reports\nMaintaining laboratory equipment by applying maintenance, qualification, and calibration plans to ensure accuracy and reliability of lab activities\nEnsuring the follow-up and progress of the investigations, change control, and CAPAs assigned to his/her perimeter, in a timely manner\nInvestigating in a timely manner and resolving any quality control events, issues, or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs\nProviding support during regulatory inspections and audits by answering to requests related to his/her perimeter\nEnsuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately\nAbout you\nBachelor's degree in science, Engineering, Industrial Engineering, or a related discipline.\nSignificant relevant experience in manufacturing quality, including demonstrable experience in managerial or leadership role is an advantage.\nStrong leadership, analytical, problem-solving, and communication skills.\nSix Sigma, or equivalent quality certification is an advantage.\nWhy choose us?\nShape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.\nTransform lives worldwide by delivering life-changing treatments anywhere, anytime.\nGrow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.\nHelp deliver 30+ new product launches by 2030, ensuring patients get treatments faster than ever.\nPursue progress, discover extraordinary\nBetter 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.\nAt 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.\nWatch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!\nThe salary range for this position is :€73 200,00 - €97 600Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. 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