2026. 01. 27. | Teljes munkaidõ | Budapest | haysWith portfolio management, technology, compliance, legal, and risk teams to develop and implement robust procedures and protocols. - Ensure compliance with internal policies and external regulations, representing the Data Operations function in audits and regulatory reviews. - Maintain strong relationships
Nézze később2026. 01. 27. | Teljes munkaidõ | Budapest | haysAnd ensure regulatory compliance, while fostering a collaborative and high‑performing team culture. Key Responsibilities - Lead, mentor, and develop a team of Trade Operations professionals, ensuring strong coverage across all operational areas. - Oversee the full trade lifecycle, including trade affirmation
Nézze később2026. 01. 27. | Teljes munkaidõ | Budapest | haysOperations. The Manager will uphold operational excellence, strengthen risk controls, and ensure regulatory compliance while fostering a collaborative, high‑performing team environment. Key Responsibilities - Lead, coach, and develop a team of Trade Operations professionals, ensuring strong coverage across
Nézze később2026. 01. 26. | Teljes munkaidõ | Budapest | PwCFor smooth vendor releases and service deployment. Spearhead security audits and ensure regulatory compliance. Day-to-Day Responsibilities Master the ServiceNow platform, resolving bottlenecks and optimizing performance. Handle incident escalations and manage change implementations. Develop and deploy
Nézze később2026. 01. 26. | Teljes munkaidõ | ICONResearch Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data. What you will be doing - Working
Nézze később2026. 01. 26. | Teljes munkaidõ | ICONA Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You
Nézze később2026. 01. 25. | Teljes munkaidõ | Miskolc | SanofiTime in compliance with regulation Nominate Quality person for batch disposition Representing Site Quality in front of Health Authorities Ensuring application and maintenance of the site manufacturing license Driving site inspection readiness Developing and engaging site quality team with the right
Nézze később2026. 01. 25. | Teljes munkaidõ | Budapest | ParexelWhen our values align, there's no limit to what we can achieve. Are you passionate about regulatory affairs in the life science industry? Do you thrive in a dynamic team environment and enjoy managing complex projects? Parexel is seeking a talented (Senior) Regulatory Affairs Consultant with CMC
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