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Our client is a well established Global manufacturer of power generation/turbines/combustion to a myriad of industries including Marine, Petrochemical, Waste to Energy, Hospitals, Education, Offshore Oil & Gas, Power Generation, etc.
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Compile clinical evidence from multiple sources such as current and past clinical trials, post market clinical follow up data and literature review updates, ad-hoc analysis, meta-analyses, or other sources of safety and performance data (e.g. investigator-initiated study clinical data) and synthesize the information in support of European Medical Device Regulation (EU MDR.
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Familiarity with Federal Aviation Administration(FAA) and European Aviation Safety Agency (EASA)requirements. Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry.
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Oversee the companys adherence to domestic and international regulatory standards, including FDA regulations, ISO standards, ASTM, and European Medical Device Regulation, for medical device design and development.
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The inspiration of Svetness was born in Europe and utilizes the healthy European Life. Our mission is to be the best personal training company in the World by providing superior training, nutrition and next generation service to our Global Clients.
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Our products are used by some of the world's leading organisations, such as Deutsche Bank , UBS , the European Commission , and others. We’re an ambitious VC-backed startup, with leading global investors including IQ Capital , Seedcamp , and Deutsche Bank.
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Biospan is now an established company/start-up operating in the United Kingdom, the United States, the European Union, and the Middle East. We are a Bio-Tech company and require an experienced Technology executive to execute our innovative direction and help us scale our global operations and product vision with the full force of today's tools, including artificial intelligence and LLMs.
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Société Generale, a leading European bank, and AllianceBernstein, a leading global investment management and research firm, announced their plans to form a joint venture combining their cash equities and equity research businesses under the name BernsteinSG.
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Provide support for common and advanced network' administrative tasks related to the European network environment including backup and restore, Port changes to switches, Router Interface creation ,QOS and routing modification.
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Curaleaf International is the largest vertically integrated cannabis company in Europe with a unique supply and distribution network throughout the European market, bringing together pioneering science and research with cutting-edge cultivation, extraction and production.
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Social Impact: Ten employee-driven Business Resource Groups; two paid volunteer days annually; Environmental, Social and Governance (ESG) initiatives for local and global impact. Working knowledge of US, Canadian and European accounting and bankruptcy controls and laws.
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Responsibilities: Install, configure and support LAN,WAN,Wlan and telephony communications systems in a large enterprise and factory environment for a global corporation. Detailed Job Description: Seeking an experienced Network Engineer to join our IT Global Infrastructure team.
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Credit Suisse Asset Management LLC’s Regulatory Reporting Team has the responsibility for the Division’s regulatory reporting requirements, primarily in the US, including Forms PF, PQR, ADV, TIC, and FATCA/CRS and regulatory requirements in the European Union, i.e. AIFMD and MiFID II. The Team mainly covers the Dodd-Frank requirements and hedge fund and commodity pool regulations in addition to certain tax functions.
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Work collaboratively and proactively with other GXO tax teams including SALT, European, indirect, planning and global tax provision. Our greatest strength is our global team energetic, innovative people of all experience levels and talents who make GXO a great place to work.
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Post -graduate patient-care experience preferredRegulatory knowledge: Familiarity with global regulatory guidance especially International Conference on Harmonization (ICH), Food and Drug Administration (FDA) and European Medicines Agency (EMA) relevant to clinical and safety data and clinical development and labelling.
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