{"id":44824,"date":"2026-06-24T09:44:00","date_gmt":"2026-06-24T09:44:00","guid":{"rendered":"https:\/\/safeness.com.tn\/courses\/iso-iec-170252017-lead-auditor-laboratoires\/"},"modified":"2026-08-11T12:23:51","modified_gmt":"2026-08-11T12:23:51","slug":"isso-iec17025-2017-lead-auditor-quality-management-system-fr","status":"publish","type":"lp_course","link":"https:\/\/safeness.com.tn\/fr\/courses\/isso-iec17025-2017-lead-auditor-quality-management-system-fr\/","title":{"rendered":"ISO\/IEC 17025:2017 Lead Auditor \u2014 Laboratoires"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"44824\" class=\"elementor elementor-44824 elementor-42728\" data-elementor-post-type=\"lp_course\">\n\t\t\t\t<section class=\"elementor-element elementor-element-fd8d863 e-flex e-con-boxed e-con e-parent\" data-id=\"fd8d863\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-100ecdf elementor-widget elementor-widget-heading\" data-id=\"100ecdf\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h6 class=\"elementor-heading-title elementor-size-default\">FORMATION CQI &amp; IRCA<\/h6>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-8e6a3bc elementor-widget elementor-widget-heading\" data-id=\"8e6a3bc\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Pr\u00e9sentation du cours<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-5ac2a11 elementor-widget elementor-widget-text-editor\" data-id=\"5ac2a11\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ul><li><strong>LANGUE DE FORMATION : <\/strong>anglais et fran\u00e7ais<\/li><li><strong>ATOUTS ET B\u00c9N\u00c9FICES : <\/strong>acqu\u00e9rir des comp\u00e9tences d&#8217;audit de premier plan et engager votre parcours vers la certification d&#8217;auditeur tierce partie.<\/li><li><strong>CERTIFICATION DU COURS :<\/strong> cette formation est pleinement reconnue par le CQI &amp; IRCA.<\/li><li><strong>M\u00c9THODE P\u00c9DAGOGIQUE : <\/strong>70 % d&#8217;apports du formateur, 30 % de jeux de r\u00f4le et d&#8217;\u00e9tudes de cas.<\/li><li><strong>PR\u00c9REQUIS : <\/strong>les participants doivent conna\u00eetre les exigences de l&#8217;ISO\/IEC<\/li><\/ul><p>17025:2017, ou avoir suivi une formation reconnue aux fondamentaux du SMQ bas\u00e9e sur l&#8217;ISO\/IEC 17025:2017 avant de s&#8217;inscrire.<\/p><ul><li><strong>PR\u00c9SENTATION : <\/strong>d\u00e9velopper les comp\u00e9tences pour auditer de mani\u00e8re professionnelle un syst\u00e8me de management de la qualit\u00e9 et \u00e9valuer objectivement la conformit\u00e9<\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/section>\n\t\t<section class=\"elementor-element elementor-element-ba0a8dd e-flex e-con-boxed e-con e-parent\" data-id=\"ba0a8dd\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-4e7696b elementor-widget elementor-widget-heading\" data-id=\"4e7696b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">D\u00e9tails du programme<\/h2>\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-9d9f3ef e-flex e-con-full e-con e-parent\" data-id=\"9d9f3ef\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-ccb309f e-flex e-con-full e-con e-parent\" data-id=\"ccb309f\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t<div class=\"elementor-element elementor-element-8cb96fb elementor-widget elementor-widget-text-editor\" data-id=\"8cb96fb\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p>des laboratoires aux exigences des organismes d&#8217;accr\u00e9ditation, gr\u00e2ce \u00e0 notre formation ISO\/IEC 17025 Lead Auditor certifi\u00e9e CQI et IRCA.<\/p><p>Les participants \u00e0 cette formation approfondie apprennent \u00e0 conduire des audits internes et externes de syst\u00e8mes de management de la qualit\u00e9 selon l&#8217;ISO\/IEC 17025. Ils d\u00e9veloppent les connaissances et comp\u00e9tences pour :<\/p><ul><li>Planifier, conduire, rapporter et suivre des audits internes et externes selon l&#8217;ISO 17025, conform\u00e9ment aux normes ISO 19011 et ISO 17021 selon le cas<\/li><li>Promouvoir le r\u00f4le de l&#8217;audit dans le programme global de management de l&#8217;organisation, ainsi que le r\u00f4le des auditeurs dans l&#8217;am\u00e9lioration de la conformit\u00e9 et de la comp\u00e9tence des laboratoires<\/li><li>Cette formation pratique, intensive et tr\u00e8s interactive de 5 jours s&#8217;articule autour d&#8217;une \u00e9tude de cas centrale et d&#8217;ateliers, permettant aux participants de mettre en pratique leurs nouvelles comp\u00e9tences.<\/li><li>Les participants satisfont aux exigences de formation formelle permettant d&#8217;\u00e9voluer vers le statut de CQI and IRCA Registered QMS Lead Auditor. L&#8217;\u00e9valuation combine contr\u00f4le continu et examen \u00e9crit.<\/li><\/ul><p><strong>TH\u00c8MES ABORD\u00c9S :<\/strong><\/p><ul><li>La qualit\u00e9 et son assurance<\/li><\/ul><p><strong>&gt;<\/strong> Introduction \u00e0 l&#8217;audit<\/p><p><strong>&gt;<\/strong> L&#8217;ISO 17025 et les autres normes ISO<\/p><p><strong>&gt;<\/strong> Les syst\u00e8mes documentaires<\/p><p><strong>&gt;<\/strong> La planification de l&#8217;audit<\/p><p><strong>&gt;<\/strong> La liste de v\u00e9rification<\/p><p><strong>&gt;<\/strong> Les r\u00e9unions d&#8217;ouverture<\/p><p><strong>&gt;<\/strong> La r\u00e9daction des non-conformit\u00e9s<\/p><p><strong>&gt;<\/strong> Les techniques d&#8217;audit<\/p><p><strong>&gt;<\/strong> Les r\u00e9unions de cl\u00f4ture<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-b590db5 e-flex e-con-full e-con e-parent\" data-id=\"b590db5\" data-element_type=\"container\" data-e-type=\"container\" data-settings=\"{&quot;background_background&quot;:&quot;classic&quot;}\">\n\t\t\t\t<div class=\"elementor-element elementor-element-7e1a597 elementor-widget elementor-widget-text-editor\" data-id=\"7e1a597\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><strong>&gt;<\/strong> La r\u00e9daction du rapport d&#8217;audit<\/p><p><strong>&gt;<\/strong> La r\u00e9union de cl\u00f4ture<\/p><p><strong>&gt;<\/strong> Le suivi et les actions correctives<\/p><p>Audits de premi\u00e8re, deuxi\u00e8me et tierce partie<\/p><p><strong>COMMENT SUIS-JE \u00c9VALU\u00c9 ?<\/strong><\/p><p>Le participant est \u00e9valu\u00e9 sur sa participation et sa performance tout au long de la formation : exercices, jeux de r\u00f4le, \u00e9tudes de cas et l&#8217;ensemble des activit\u00e9s. La pr\u00e9sence \u00e0 la totalit\u00e9 de la formation est obligatoire.<\/p><p>Un examen \u00e9crit de 2 heures a lieu en fin de formation. Il se d\u00e9roule \u00e0 livre ferm\u00e9 : le participant peut uniquement utiliser son exemplaire des normes internationales concern\u00e9es, ou un dictionnaire si la langue de formation n&#8217;est pas sa langue maternelle. La note minimale de r\u00e9ussite est de 70 %.<\/p><p><strong>PUBLIC CONCERN\u00c9<\/strong><\/p><p>Cette formation s&#8217;adresse aux personnes travaillant dans des organisations souhaitant exploiter des syst\u00e8mes de management de laboratoire efficaces, notamment :<\/p><ul><li>Celles qui souhaitent r\u00e9aliser des audits de premi\u00e8re, deuxi\u00e8me ou tierce partie selon l&#8217;ISO 17025<\/li><\/ul><p><strong>&gt;<\/strong> Responsables qualit\u00e9 et responsables techniques de laboratoire, techniciens et superviseurs<\/p><p><strong>&gt;<\/strong> Auditeurs qualit\u00e9 fournisseurs souhaitant \u00e9valuer des prestataires de services de laboratoire<\/p><p><strong>&gt;<\/strong> Auditeurs en activit\u00e9 souhaitant \u00e9largir leurs comp\u00e9tences<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/section>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Une formation Lead Auditor ISO\/IEC 17025 d\u00e9veloppant les comp\u00e9tences n\u00e9cessaires pour \u00e9valuer la comp\u00e9tence, l\u2019impartialit\u00e9 et la coh\u00e9rence des activit\u00e9s de laboratoire.<\/p>\n","protected":false},"author":2,"featured_media":45006,"comment_status":"open","ping_status":"closed","template":"","course_category":[],"course_tag":[],"class_list":["post-44824","lp_course","type-lp_course","status-publish","has-post-thumbnail","hentry","course"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v28.2 (Yoast SEO v28.2) - 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