2026. 03. 22. | Teljes munkaidõ | ParexelWhen our values align, there's no limit to what we can achieve. Parexel is seeking an experiencedAssociate Project Directorto lead our Regulatory Affairs Consulting teams and deliver exceptional solutions to our clients. In this pivotal role, you will combine advanced Regulatory Affairs expertise
Nézze később2026. 03. 22. | Teljes munkaidõ | ParexelAnd evaluate new and updated regulations, guidelines, standards, and procedural changes issued by health authorities across assigned regions. Conduct impact assessments to determine how regulatory changes may affect the organization’s products, filings, labeling, clinical requirements, and lifecycle strategies
Nézze később2026. 03. 22. | Teljes munkaidõ | Budapest | ParexelTo work. We are unable to provide visa sponsorship or relocation support for this role. About the Role We're looking for an experienced Audit Specialist to lead Sponsor Audits and Regulatory Inspections across our European operations. You'll provide expert guidance to project teams, drive audit
Nézze később2026. 03. 21. | Teljes munkaidõ | Budapest | WerfenFeasibility against applicable regulations in targeted markets, under supervision Contributing to the preparation and maintenance of regulatory documentation (e.g. Design History Files, Technical Documentation) Supporting the maintenance of regulatory profiles for assigned IVD medical devices Assisting
Nézze később2026. 03. 20. | Teljes munkaidõ | Budapest | MET GroupSupport Group Market Risk in enhancing risk models, analytics, and reporting tools to optimize monitoring Conduct advanced risk assessments, including VaR back-testing, sensitivity analyses, and scenario simulations Participate in model validation processes and ensure compliance with regulatory
Nézze később2026. 03. 20. | Teljes munkaidõ | Budapest | SogelinkDedicated to managing commercial public domain occupancy. It digitalizes permits, market rights, fee collection, and regulatory workflows within an MVC-based platform, with dedicated APIs supporting mobile and tablet clients. As part of our Ambition 2030, the platform is evolving towards a modern
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | EYProcesses, and design and implement systems to effectively manage these areas governed by regulatory bodies globally (FDA, EMA, etc.). Do you have consulting and Safety systems experience and a passion for helping customers optimize their Pharmacovigilance (PV) processes? As a Safety Consultant, you
Nézze később2026. 03. 19. | Teljes munkaidõ | Budapest | ContinentalOf internal control systems and compliance with internal standards - policies and regulatory requirements. Compile audit report and present the results to the management Propose measures to address identified risks and provide actionable advice to the business. Advise management on the development
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