לחברת it מובילה דרוש/ה מהנדס/ת מערכת ipt
"לחברת IT מובילה דרוש/ה מהנדס/ת מערכת IPT At least CCNP VOICE, preparing for CCIE voice At least 3 years of network engineering and services experience in large, complex environments Ability to configure systems and integrate them with other communications systems Experience working with vendors on system installations and software and hardware upgrades Ability to diagnose complex problems and implement fixes in a multivendor environment; Familiarity with basic networking technologies including IP routing, VLANs, DHCP and HTTP Substantial experience with Cisco Unified Communications systems including CUCM, Unity Connection, UCCX, CUPS, CUBE,, and voice gateways; Strong understanding of VoIP technologies including Cisco SCCP and IETF SIP and related protocols; Extensive hands-on experience with SIP trunking and debugging SIP messaging; Ability to work and communicate effectively with customers, assessing their needs, and analysing and resolving their problems Ability to work both independently and as a part of a team Understanding and ability to document processes and work plans מיקום: מרכז נא לשלוח קורות חיים לאיציק הברברג "
לטלדור דרוש/ה תוכניתן/נית rt embedded
"לטלדור דרוש/ה תוכניתן/נית RT EMBEDDED ניסיון בפיתוח embedded מונחה עצמים OOP ו- C ++ ידע וניסיון ב- VXWORKS על מעבדי POWER –חובה. משרה מלאה עבודה באיזור הצפון. נא לשלוח קורות חיים לאיציק הברברג "
לפרטים הצטרף לקבוצה הגדולה בארץ לחיפוש עבודה
"דרוש/ה תוכניתן/ת SQL .שליטה מלאה בפיתוח SQL – חובה לפחות שנתיים ניסיון בתחום – חובה ידע בגולדפלוס / דולדמיין – יתרון הכרות עם תהליכי חסכון ארוך טווח – יתרון יכולת עבודה בצוות יכולת עבודה בלחץ יחסי אנוש טובים העבודה בתל אביב נא לשלוח קורות חיים לאיציק הברברג "
דרוש/ה מומחה/ית ui/ux לחברת טלדור
"דרוש/ה מומחה/ית UI/UX לחברת טלדור - ניסיון של 3 שנים ומעלה בעיצוב UI ו-WEB - ניסיון ב-JAVASCRIPT/HTML5 - ניסיון קודם בבניית PROTOTYPE, LAYOUT מיקום: מרכז נא לשלוח קורות חיים לאיציק הברברג "
"Multi talented Backend Lead A dynamic, innovative and exciting startup that is shaping the future of how people will manage their day to day life is expanding. We are looking for bright and creative developers who will be responsible for the architecture, design and development of our product. You will make your mark on a revolutionary product that is solving a real problem people have in their day to day life and will join a seasoned team for a great experience throughout the way. Multi talented back-end lead Job requirements: • Hands-on experience building web services and specifically back end experience. · Experience building consumer facing products or services. • Experience with open source web applications frameworks. Node.JS is a big advantage. • Hands-on experience building and integrating with mobile applications (Advantage). • Experience with building cloud IT services. • Familiarity with information security vulnerabilities and risk management. • Can thrive in an ultra-dynamic startup environment. • Must be proactive, self-directed, detailed, out of the box thinker, and organized. send CV to "
"Microsoft Services help customers realize their full potential through accelerated adoption and productive use of Microsoft technologies. We are a global team of exceptional people who deliver world class services with partners, earning customer Confidence, trust, and loyalty by Improving the overall Customer and Partner Experience, Serving as the customer advocates within Microsoft and Driving customer-centric product improvement. The TAM: • Is the trusted advisor to developers, architects and key decision makers .He will build a relationship to understand their priorities, challenges and technical goals • The TAM will have access to the local team, the wider Microsoft UK technical community and a global network of expertise in order to deliver on the goal of improving the quality of software delivery for clients. • The TAM Will build and own a delivery plan which includes: strategic advice, solution Architecture assessments, workshops, prototyping, design reviews, code reviews, performance Benchmarking, and general development consultancy. The impact of the delivery plan will generate high levels of satisfaction through the value customers recognize to their business over an extended, long term engagement. Skills and qualifications: • IT industry background working with software development or solution delivery • Comfortable working face to face with clients at varying levels within organisations • Strong time, project and priority management skills • Degree or equivalent in Computer Science, Engineering • Demonstrable knowledge in key technologies and techniques for delivering software such as: o Development Languages (C#, , C++, TSQL) o .NET technologies up to .NET 4.5 (WCF, WF, MVC) o Server Systems (Azure, BizTalk, SQL, SharePoint, AppFabric, Dynamics) o Client Systems (WPF, HTML, Metro) o Application Lifecycle Management (Agile, SCRUM, TFS) o Solution Architecture (SOA, enterprise architectures)"
"מעל 5 שנות ניסיון בניהול איכות ורגולציה בחברות המפתחות ומייצרות מכשור רפואי ניסיון במכשור רפואי מושתל אנגלית שפת אם "
"Clinical Trials: • Overall responsibility and monitoring clinical trials including trials for regulatory approvals and marketing purposes • Identify together with marketing key scientists and medical researchers that can add to the art and practice of patient care related to products • Oversee and ensure all research activities are in compliance with GCP Guidelines (FDA), HIPAA, Helsinki, and other international research governing bodies • Develop and maintain liaison among outside physicians, preclinical/ clinical investigators, CRO's to initiate and expedite clinical studies • Work with the Chief Medical Officer in the development of research strategy, tactics and research budget planning Regulatory Affairs: • Manages the US and international regulatory affairs activities according to U.S. Government policies, (FDA); applicable State requirements; and European and international regulations and standards. • Management of clinical SOP's and assurance of training to them within the company and at clinical sites • Recognize potential regulatory issues in day-to-day activities, from product development through the manufacturing process • Responsible for regulatory issues of product lines and assure product and product labeling is in compliance with all regulatory requirements • Review all clinical study protocols for compliance with FDA, European and international regulations and standards. • Review ECO's for regulatory compliance • Participates in risk management activities related to product safety Requirements & Skills • B. Sc. or higher in life sciences • 5-10 years of clinical studies experience with medical devices required • Preferable formal education and/or training in FDA and EMEA regulation, CRA, GMP, GLP • Familiar with laws governing the conduct of clinical studies and with completing 510(k) Statements, PMAs, study protocols, investigational plans, patient case report forms and informed consents • Experience in managing regulatory approvals of medical products in the US and Europe. PMA products experience a significant advantage. • Excellent oral and written English • Highly organized and detail oriented, with solid analytical and interpersonal skills • Project management skills • Ability to effectively handle multiple priorities in a fast paced, action oriented team environment Email for CV's "
medical director - based in the us - ny nj
"- Pharmacovigelence ( prime objective with proven track record )/ product safety - Medical coordination with all clinical aspects related to the product and the clinical study - Interacting with KOL's and principle study's investigator, to support the Understanding of the technology and get their utmost cooperation. - Generating scientific evidence to establish the product awareness and positioning - Product training and participating in clinical site initiation Background - MD with experience in Pharmacovigelence - Experience in wound care advantage to NJ based candidates Reporting to the CEO. Email for CV's - "
vp regulatory affairs biomed arena
"A promising advanced Biomed SU company is seeking a VP Regulatory affairs, Biomed arena Based in the US (NY - NJ)!!! Responsible for all regulatory activities (e.g., pre-IND documents and meetings, IND submissions, IRB submissions, etc.), including the following: • Leading and identifying optimal development of regulatory pathways • Overall responsibility for, and active participation in, preparing all regulatory aspects of scientific reports and protocols • Coordinating all activities related to the above (together with the relevant groups within the company, including research, development, CMC, pre-clinical and clinical) • Assisting with development of clinical programs • Overall responsibility for: o Documentation center o All reporting to the regulatory authorities o QA group Email for CV's - "
לפרטים הצטרף לקבוצה הגדולה בארץ לחיפוש עבודה
dudamobile is offering $2,500 if you help hire an experienced web developer .
"Click to learn more about how we can help you search your friends to find a match. You can receive $1,250 if a friend of a friend is hired. For more information: "
looking to launch your start-up to the us/ international markets?
"A business development (sales and marketing management) veteran/ expert to the US and International markets is offering to help launch your sales and marketing efforts. Reach me on my mobile: 058-4785492 / Dom"
java/j2ee developer looking for a job
"J2EE and Java Developer, Computer Science (Honors) Major. 3+ years experience in development of end-to-end Java/J2EE sites, Server/Client side development. Experience with Java, JSF, SQL, Eclipse, Toad, JDBC, Oracle, CSS/HTML, Ajax, Tomcat, Servlets, XML. Creative approach to challenges, a team player, independent and self motivation ability. Looking for a JAVA\J2EE position."
כל הפרטים בקבוצת משרות הייטק בין חברים
assistant controller cpa for a global company
"דרוש/ה עוזר חשב מנוסה ורציני בעל הסמכה ורישיון CPA !!! נדרש ניסיון עבודה בחברה גלובאלית - לא ישראלית נדרש ניסיון בניהול קבוצת עובדים יתרון ליוצא אחד מחברות ראיית החשבון הגדולות - BIG5 אנגלית ברמת שפת אם פרופיל אישי- טיפוס נמרץ . רציני ובעל מוטיבציה גבוהה Expiring in 12 days"
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