28.05.2024 | Full-time | SAPChallenges. What you bring Key Responsibilities Serve as single point of contact (SPOC) for integration initiatives, ensuring seamless collaboration and communication across teams. Oversee security, compliance and archiving concepts, implementing measures to safeguard sensitive data and ensure regulatory
Uita-te mai târziu28.05.2024 | Full-time | TideMeet and exceed our regulatory are committed to a 100% Infrastructure-as-Code approach to infrastructure builds using Terraform and currently deploy to AWS. We also follow the GitOps model of application deployment and use tools such as ArgoCD, Helm and Crossplane to facilitate
Uita-te mai târziu28.05.2024 | Full-time | NRLStandards. - Document test results, identify deviations, and recommend corrective actions. 3. *Stakeholder Engagement* - Communicate with project stakeholders (clients, contractors, regulatory agencies) to provide updates on commissioning progress. - Address any concerns or issues related to commissioning
Uita-te mai târziu28.05.2024 | Full-time | Signant HealthTeam is accountable for successful delivery of localisation activities, to meet key project milestones, whilst adhering to Good Clinical Practice (GCP), Signant Health processes and regulatory compliance. Prior knowledge of handling multi and complex tasks, on a volume of projects is seen as an asset
Uita-te mai târziu28.05.2024 | Full-time | IQVIAInitiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesManaging
Uita-te mai târziu28.05.2024 | Full-time | DanfossUnderstanding of EHS regulations, standards (., OSHA, ISO 14001), and industry best practices. We appreciate if you have knowledge of and experience with the following platforms/technologies Quentic, SynergiLife, ChemWatch, man-down technologies. Experience with complex IT projects from conception
Uita-te mai târziu28.05.2024 | Full-time | IQVIAAs perform additional tasks as deemed appropriate by Line ManagerREQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good understanding of the regulations, directives and guidance supporting clinical Research and DevelopmentDemonstrates comprehensive regulatory/technical expertise Good negotiating skills
Uita-te mai târziu28.05.2024 | Full-time | F063 DB Global Technology SRLOf Information Security and with preference to prior experience in IS.Very strong ability to work focused and in a systematic way with only limited guidance and - in particular, under time pressure - exceptional attention to detailExcellent working experience of risk management, regulatory and senior stakeholder
Uita-te mai târziu28.05.2024 | Full-time | ProductLife GroupLtd’s Quality Management System Group 11 Education Bachelor’s degree in a science related field, or A levels with data entry experience Group 12 Experience Experience of 1-3 years of RA experience in the pharmaceutical or service industryKnowledge in EU regulations Group 13 Skills Excellent
Uita-te mai târziu28.05.2024 | Full-time | Chronos ConsultingThe qualification - development of employees within the teamDemonstrate strong project management skills with the ability to take initiative and drive projects to completion within budget and schedule to meet corporate requirementsEnsure compliance with regulatory framework and standardsGenerate and validate
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