Ph3Sterile Manufacturing | French-Speaking | GMP | Pharma /h3 pOn behalf of our client, a well‑established and steadily growing pharmaceutical company with a strong reputation in bsterile manufacturing and clinical supply /b, we are seeking an experienced bDeputy Qualified Person (QP) /b to strengthen the Quality Assurance team. /p pThis is a permanent opportunity within a close‑knit, family‑style organisation, offering hands‑on impact, visibility, and the chance to actively shape quality and compliance standards in a dynamic GMP environment. /p h3Your Key Responsibilities /h3 ul liAct as Deputy to the QP, including batch certification under delegated responsibility /li liReview and approve quality documentation in line with GMP requirements /li liMaintain strong shop floor presence, ensuring compliance and identifying improvement opportunities /li liAct as the main compliance interface for clients and external partners /li liDrive and support Change Control processes and continuous improvement initiatives /li liLead and manage deviations and investigations /li liProvide QA support across production, laboratories, and warehouse operations /li liPrepare and review certificates and client‑facing documentation /li /ul h3Your Profile /h3 ul liDegree in Pharmacy, Chemistry, Life Sciences, or equivalent /li liProven experience as a QP or Deputy QP within the pharmaceutical industryMinimum 5+ years of GMP (cGMP) experience /li liStrong and demonstrable experience in sterile / aseptic manufacturing (essential) /li liExperience in team leadership or cross‑functional coordination /li liBackground in a CDMO environment is highly advantageous /li liFluent French (C1 or higher) is mandatory, with excellent written communication skills /li liStrong command of English /li liConfident user of standard IT tools (e.g., MS Office) /li /ul h3Why This Opportunity? /h3 ul liJoin a growing pharmaceutical company with international exposure /li liWork in a people‑oriented, agile environment with short decision paths /li liTake on a high‑impact QA role with real ownership and visibility /li liBe part of an organisation active in clinical development and innovative pharmaceutical manufacturing /li /ul /p #J-18808-Ljbffr