13 resultaten voor Audits in Charleroi binnen een straal van 30 km

You will contribute the preparation of audits (internal/external, regulatory inspections). * Coordinate the development local instructions, liaise with key stakeholders in order to maintain common practices with regards to internal audit within development entities, coordinate and update the development internal audit schedule, ensuring appropriate application of the audit planning and also manage Self inspections in the Lab.
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Partner with CS Compliance to coordinate the audit/inspection preparation for CPLO. Timely and suitable Audit preparation (internal, Corporate or by the authorities), execution, support and follow up leading to successful outputs. * Analyze internal/external audit and other monitoring results with a view to identifying priorities for the further development of compliance actions.
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Stuur me nieuwe vacatures per e-mail.

Be the central QA point of contact for the organization for investigations / deviations / out-of-specifications / audit observations associated with the assigned vendors. * Have the overview of the company audit and HA inspections related to the vendors. Track and follow-up on Audit observation and CAPA plan implementation at the vendor. * Support on customer audits and Health Authority inspections at the vendors, as needed
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data entry performance of audit reports and CAPAs in the Veeva audit system. * Enable insights for the company through data collection, entry, and analysis in the audit * Curate data, including quality checks of audit management tool as needed, for * Management System (includes data entry of audit related information and data * Make extractions from the audit management tool for data inclusion within internal * Act as a key point of contact in Global Quality Auditing & Compliance team for the audit management tool.
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Nos missions portent sur : l'étude d'amélioration d'installations existantes ou l'implantation de nouvelles installations, sur des travaux de recherches, d'audits techniques, des missions de maintenance, d'études, de conception et d'exécution, de planification, de gestion de chantier ainsi que du contrôle de réalisations dans les pôles d'activité tels que le génie civil, la construction mécanique et métallique, les techniques spéciales, l'électricité, le piping,etc...
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We hebben je zoekopdracht uitgebreid met 6 vacatures buiten de geselecteerde regio

Als Lead Auditor Information Security (M/V/X) kom je terecht in een team van auditoren, met verschillende expertises, dat zich elke dag inzet voor een steeds veiligere & efficiëntere samenleving. Onze klanten situeren zich over heel België, maar houden we zoveel mogelijk rekening met jouw regio bij het inplannen van audits. Er wordt een klantenportefeuille toegewezen o.b.v. jouw interesses & ervaring, met een focus op audits over informatiebeveiliging (ISO27001) en kwaliteit (ISO9001).
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Als QSE (Quality Safety & Environment) Auditor (M/V/X) kom je terecht in een team van auditoren met elk zijn eigen expertises. Als QSE Auditor (M/V/X) ben je verantwoordelijk voor het organiseren & uitvoeren van auditopdrachten bij de klanten in de aan jou toegewezen klantenportefeuille. Deze auditopdrachten situeren zich binnen de domeinen kwaliteit (ISO9001), veiligheid (OHSAS, VCA) en milieu (ISO14001). * Tijdens deze audits leg je vlot contact met alle betrokken partijen: directie, management en medewerk(st)ers.
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Notre client est à la recherche d'un Project Manager Engineering Capex à consonnance technique pour driver un de leurs projets clefs. * Leader les achats (la négociation se faisant via le procurement manager), * Expérience avérée en gestion de projets CAPEX industriels, idéalement dans un environnement pharmaceutique, chimique ou biotechnologique. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - Le projet concerne la distribution centralisée de solvant dans le bâtiment upstream. Il souhaite retirer les fûts de solvant de la zone de production et centraliser leur alimentation via des cuves tampons, et de manière automatisée. * Comprendre et driver les aspects techniques de ce projet (et leader une équipe composée
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Work closely with Clinical Manufacturing Teams to ensure that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way. * More specifically, provide quality support for qualification and validation activities related to Clinical Manufacturing activities like facilities cleaning processes, viable and non-viable environmental monitoring, equipment and system qualification/validation - Ensure adequate documentation processes and systems are available and followed for development projects (SOPs / Protocols / Report review…) * Be partner with other departments to identify, mitigate and subsequently resolve complianc
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Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * S'assurer du respect cGMP. * Participer activement à la préparation des lots de process performance qualification (PPQ). * Revoir et approuver les dossiers de lot de production en version papier et électronique. * Participer à la gestion/revue/approbation des déviations. * Participer à la gestion/revue/approbation des CAPA. * Participer à la gestion/revue/approbation des change controls. * Revoir et approuver les protocoles et rapports de validation (CIP/SIP/EM/Thermal mapping). * S'assurer que les risques/non conformités identifiées sont traités de manières adéquates et remontés dans les temps. Votre profil * Diplômé(e) de l'enseignement supérieur de type Bachelier ou Master (biotechnologie, pharmacie, etc.). * Bilingue Français e
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Work collaboratively as part of a wider team and when required deputise for the of Bio MSAT Quality and other Bio MSAT Quality Leads * Process industrialization and Technical transfers within commercial manufacturing facilities * Build, establish and develop a governance model and process for Quality oversight of Internal and External MSAT for Bio Drug Substance and Drug Products which fosters continuous quality process improvement, optimized resource utilization and key indicator based performance monitoring * Promote quality best practices throughout the External & Clinical Supply Quality team and where possible business stakeholders. * Knowledge in multiple areas of Biopharma incl manufacturing and analytical testing, including the
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Proven experience in data validation, preferably in a regulated environment. * Validate the integrity of transferred and transformed data in the new system. * Draft and execute validation protocols (tests, reports, documentation). * Collaborate with IT and business teams to guarantee data accuracy and consistency. * Manage a backlog of dashboards awaiting validation and ensure effective follow-up. * Strong proficiency in SQL for executing tests and validating data. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Define User Requirement Specifications (URS) and ensure compliance. * Communicate with various (IT, Business, QA, QC). * Be proactive in coordinating ta
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Expertise in lab relocation is a plus - Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Lead and coordinate the laboratory expansion and modernization project. * Manage commissioning and qualification activities for equipment and installations. * Collaborate closely with various internal departments and international . * Ensure compliance of facilities and processes with regulatory standards (GMP Pharma). * Identify technical needs and propose appropriate solutions. * Monitor project progress, manage risks, and maintain regular communication with . Votre profil * Bachelor degree with 5 years of relevant experience or Master's degree with 3 years of relevant experience; degree in science, engineering, or a related field. * Pharma skills (change request, deviation
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