2026. 02. 26. | Teljes munkaidõ | Budapest | Telio Management GmbHAnd internal platform capabilities - Participate in improving CI/CD pipelines and DevOps maturity - Contribute to observability, monitoring and reliability improvements - Ensure high standards of code quality, maintainability and security - Support integration with telephony, VoIP, financial and regulatory
Nézze később2026. 02. 26. | Teljes munkaidõ | Budapest | Citibank Europe plc HungaryBash, PS). Strong knowledge and experience of PKCS protocols, JCE and CSP/KSP Work with and understand regulatory and risk management requirements Strong security mindset Any experiences with Hardware Security modules Programming skills in most common languages (, C+, C#, Python, Perl, Java) is a plus
Nézze később2026. 02. 26. | Teljes munkaidõ | Budapest | Wolters KluwerMajor & Strategic Account Executive (Libra Legal AI Assistant) As a Major & Strategic Account Executive, you will be working in our Legal & Regulatory division where we help legal and compliance professionals enhance productivity, mitigate risk, and solve complex problems confidently
Nézze később2026. 02. 26. | Teljes munkaidõ | Budapest | Baker McKenzieDiligence processes Assist in regulatory matters Support with client communication, meeting preparation, and matter management. Ensure accurate drafting, version control, and transaction administration throughout deal execution. Requirements Professional Qualifications Hungarian law degree with strong
Nézze később2026. 02. 25. | Teljes munkaidõ | Budapest | ClarioJoin our Hungary team as a Quality Assurance Auditor, Supplier Quality in full time (40h/week)to support the supplier quality management program. Help to ensure the highest level of supplier quality and delivery, with compliance to Clario procedures and applicable regulations. Support cross
Nézze később2026. 02. 25. | Teljes munkaidõ | Budapest | IQVIAAs an experienced individual contributor within IQVIA Biotech’s Regulatory Affairs team, you’ll operate under limited supervision to drive clinical trial regulatory strategy and delivery across complex, multi‑stakeholder projects. You’ll lead cross‑functional regulatory workstreams, prepare and review clinical
Nézze később2026. 02. 25. | Teljes munkaidõ | Budapest | ParexelWhen our values align, there's no limit to what we can achieve. We are seeking an experiencedSenior Regulatory Affairs Associateto lead and contribute to end-to-end (E2E) labeling process management and oversight. This critical role ensures compliant, consistent labeling operations through
Nézze később2026. 02. 25. | Teljes munkaidõ | Budapest | ICONregulations and standard operating procedures. - Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports. Your profile - Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field. - Previous experience in clinical research
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