computer

1,000 vagas de computer em Brasil. Encontre vagas atualizadas diariamente.


  • State of São Paulo, State of São Paulo, Brasil Amazon Tempo integral

    This job is with Amazon, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. DESCRIPTION: AWS Infrastructure Services owns the design, planning, delivery, and operation of all AWS global infrastructure. In other words, we're the people who keep the...


  • Brasília, Federal District, Brasil Conocophilips Tempo integral

        designing and developing new control systems;    testing, maintaining and modifying existing systems;    analysing data and presenting findings in written reports;    managing operations;    working collaboratively with design engineers, operation engineers, purchasers and other internal staff;    liaising with clients, suppliers,...


  • Sergipe, Sergipe, Brasil LatinHire Remoto Tempo integral R$ 72.000 - R$ 179.000 Contrato

    Cargo: College-level chemistry tutor em aracaju (SE) – aracaju Requisitos We are looking for tutors to solve college-level Chemistry questions in English. These questions are submitted by students, who expect a response in less than 24 hours. Tutors in this project work in freelance mode and can decide the number of hours they wish to work. Do you prefer...


  • Balneário Camboriú, Santa Catarina, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Itapevi, State of São Paulo, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Sapucaia do Sul, Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Belém, Pará, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Cachoeiro de Itapemirim, Espírito Santo, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Novo Gama, State of Goiás, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Hortolândia, State of São Paulo, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Boa Vista, Roraima, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Flores da Cunha, Rio Grande do Sul, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Itabirito, Minas Gerais, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • State of Bahia, State of Bahia, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Palmas, Tocantins, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Chapecó, Santa Catarina, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Sertãozinho, State of São Paulo, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Sinop, Mato Grosso, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Araucária, Paraná, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...


  • Cambé, Paraná, Brasil Worldwide Clinical Trials Tempo integral

    What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to...