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                          53 résultats pour HAZOP Study

                          HAZOP-expert - Projectleider procesveiligheid

                          SGS Group Belgium
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                          Als Projectleider HAZOP ben jij dé expert die industriële klanten helpt hun processen veiliger te maken. Na een korte inwerkperiode ga je zelfstandig aan de slag met HAZOP- en risicoanalyses; Minstens 2 jaar ervaring in procesveiligheid of engineering, met aantoonbare HAZOP-kennis;
                          Als Projectleider HAZOP ben jij dé expert die industriële klanten helpt hun processen veiliger te maken. Na een korte inwerkperiode ga je zelfstandig aan de slag met HAZOP- en risicoanalyses; Minstens 2 jaar ervaring in procesveiligheid of engineering, met aantoonbare HAZOP-kennis;
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                          HAZOP (Hazard and Operability Study) Als (Senior) Safety Engineer zal je werken aan safety engineering projecten, zoals: risico analyse, veiligheidsstudies- en rapporten, site visites, vergaderverslagen, specifieke studies.
                          HAZOP (Hazard and Operability Study) Als (Senior) Safety Engineer zal je werken aan safety engineering projecten, zoals: risico analyse, veiligheidsstudies- en rapporten, site visites, vergaderverslagen, specifieke studies.
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                          Leading clinical trial operations: Oversee multidisciplinary study execution, ensuring quality, timeliness, and sponsor satisfaction. * Driving operational excellence: Implement process improvements, manage resources, and optimize study planning to maximize bed occupancy and revenue. * Budget ownership: Develop and manage study budgets, monitor performance, and ensure financial alignment.
                          Leading clinical trial operations: Oversee multidisciplinary study execution, ensuring quality, timeliness, and sponsor satisfaction. * Driving operational excellence: Implement process improvements, manage resources, and optimize study planning to maximize bed occupancy and revenue. * Budget ownership: Develop and manage study budgets, monitor performance, and ensure financial alignment.
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                          • Opportunities to enhance communication and language skills, job specific and broader trainings, mentoring, self-development opportunities, tuition assistance program supporting studies with business relevance
                          • Opportunities to enhance communication and language skills, job specific and broader trainings, mentoring, self-development opportunities, tuition assistance program supporting studies with business relevance
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                          • Opportunities to enhance communication and language skills, job specific and broader trainings, mentoring, self-development opportunities, tuition assistance program supporting studies with business relevance
                          • Opportunities to enhance communication and language skills, job specific and broader trainings, mentoring, self-development opportunities, tuition assistance program supporting studies with business relevance
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                          Ensure stability analyses and clinical release for clinical phases I and II, as well as any analyses in support to process understanding (IPC test, forced degradation study, multimedia dissolution, ...)
                          Ensure stability analyses and clinical release for clinical phases I and II, as well as any analyses in support to process understanding (IPC test, forced degradation study, multimedia dissolution, ...)
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                          A degree or a degree in development (close to finalizing) in Political Science, International Relations, Law, Digital Policy, or a similar field of study AND 1- 3 years of internship / work experience.
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                          Polpo B.V. * Bruxelles * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Solliciteer als één van de eersten - Introduction - Date de début : au plus tard le 30 mars 2026 - Les candidatures de personnes ne pouvant pas commencer avant cette date ne seront pas prises en compte dans cette campagne de recrutement. Si vous êtes disponible plus tard, vous pouvez néanmoins postuler : nous conserverons votre candidature pour la phase suivante. Vos responsabilités - Au sein de l'équipe Sales Belgique & UE, le/la Business Development Manager Belgique jouera un rôle central dans le développement de Polpo en Belgique. Votre mission principale : accélérer la croissance de Polpo sur le marché belge en développant un portefeuille de nouveaux clients (entreprises, cabinets de conseil, organisations et institutions) actifs dans les affaires publiques, les politiques publiques et ...
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                          Develop scope of work for conceptual studies, develop technical specifications, assist in selection, and assure quality control of contractor's work throughout project execution. * Life Extension study of existing platforms
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                          Provide technical support to Upstream and Downstream manufacturing site Develop scope of work for conceptual studies, develop technical specifications, assist in selection, and assure quality control of contractor's work throughout project execution.
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                          PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies * Address safety issues across the study from sites and the study team * Ensure Study team compliance with FDA, EMEA, ICH and
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                          PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments * Address safety issues across the trial from sites and the study team
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                          It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. End-of-studies internship preferred.
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                          Study, design and testing of high-quality and high-performance analog, mixed-signal and high voltage integrated circuits following the internal design rules and quality regulations of ICsense
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