Ph3SME Master Batch Record Designer - PAS X /h3 pResponsibilities: /p ul liOversee and update MBRs based on manufacturing changes. /li liParticipate in MBR design workshops and informal test runs. /li liSupport and execute MBR verification protocols. /li liProvide HyperCare during site go‑live and assist with end‑user training. /li liSupport MES validation activities (IQ/OQ/PQ). /li liEnsure MBR accuracy and compliance with manufacturing processes. /li liCreate master data and manage object setup (status diagrams). /li liAdhere to global MBR design standards. /li liReview and verify executed component batch records for accuracy and compliance with GMP/GDP requirements. /li liPerform timely release of raw materials, buffers, and media in SAP in accordance with approved specifications and procedures. /li liSupport Electronic Batch Record (EBR) review activities for production operations. /li liParticipate in Quality on the Floor (QOTF), GEMBA walks, and provide real‑time guidance to operations personnel on documentation practices and GMP compliance. /li liAssist in identifying and escalating documentation or process deviations during record review or shopfloor interactions. /li liCollaborate cross‑functionally with Production, QC, and Material Management teams to resolve discrepancies or issues related to material release and batch documentation. /li liSupport QA team in continuous improvement initiatives and data gathering for metrics and trend analysis. /li liContribute to the promotion of Antaes services on top of assistance provided to clients. /li /ul pQualifications: /p ul liSuccessfully completed degree in biotechnology, biology, or engineering. /li li5+ years of experience as MBR Designer with PAS‑X 3.2 in the life sciences sector. /li liProficient in both French and English (spoken and written). /li /ul h3Talent Acquisition Specialist (360 degree) /h3 pResponsibilities: /p ul liManage the full‑cycle recruitment process including job posting, sourcing, scre...