07.09.2026 | Pełny etat | Wrocław | Randstad Polska Sp. z o.o.Communication - Hands-on experience with at least 60% of the following tech stack & frameworks - Languages C, C+, Rust, Python - Standards & Protocols ISO 21434 (Cybersecurity), ISO 26262, Classic & Adaptive AUTOSAR, MISRA C - Tools DOORS, Enterprise Architect, Git/GitLab, Jenkins, CANoe, Google Test
Zobacz później31.08.2026 | Pełny etat | Wysokie Mazowieckie | emagine PolskaServices, including configuration, administration, and troubleshooting of Cisco ASR/ISR routers, using protocols such as BGP, OSPF, MPLS. Act as Technical Lead for major incidents, with 24/7 on-call availability. Oversee Change, Release, Incident, and Problem Management processes. Handle Event
Zobacz później20.07.2026 | Pełny etat | Opole | Randstad Polska Sp. z o.o.Orders). - Invoicing and milestone billing issuing invoices according to the project schedule, preparing acceptance protocols, and proof of service documentation. - Project Manager (PM) support assisting in the preparation of commercial offers, presentations, project status reports (cockpit charts
Zobacz później01.01.2012 | Pełny etat | Małopolskie | Hays PolandAccording to Standard Operating Procedures and GCP Guidelines Experience - Skills Required · Minimum of 3 years of clinical research monitoring experience · Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP. · Experience in cardiology essential · Good
Zobacz później01.01.2012 | Pełny etat | Power Media S.A.Praca w obszarze R&D telewizji cyfrowej polskiego oddziału niemieckiej firmy polegająca na rozwoju oprogramowania dla odbiorników działających w technologii Digital Video Broadcast i technologii Internet Protocol Television - rozwijanie i implementacja oprogramowania głównie w języku C/ C
Zobacz później01.01.2012 | Pełny etat | Mazowieckie | Hays PolandAre protected, and that the reported data are correct, complete and verifiable by comparing with the original documents. Furthermore, it is a responsibility of the SCRA to assure that the clinical trial is being performed according to the valid trial protocol, amendments, ICH-GCP guidelines and legal
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