mentor graphics is looking for a cpa part time job (50%) – temporary for 5 months:
"1. CPA license, at least 2 years of experience as a local controller in Israeli company/or performing a controllership roll in an outsourced service agency- preferable 2. Good knowledge and experience in – a. Dealing with local authorities (I.E. ITA, VAT, Deductions, SS) b. WTH tax regulations c. Preparation of VAT returns and good knowledge of VAT regulations d. Dealing with AP, local banks, knowledge in payments and AP/Bank reconciliations e. Knowledge in statutory reports preparation and submissions F. US GAAP – Advantage 3. Fluent English/Hebrew (reading and speaking skills) - Must Location: Rehovot with partial visits to our local office in Herzelia. Please send CV to: "
sw applications / gui programmer-jerusalem
"SW applications / GUI programmer Required skills: - Net 4.0/4.5 - Knowledge in C# (at least 2 years of proven experience) , LINQ/Lambda, Generics, Async Programming - WPF/Xaml (at least 2 years of proven experience), MVVM - Communication protocols knowledge – advantage - Video Streaming experience – advantage"
לחברת הייטק דרוש/ה web developer קו"ח:
"• 2 years of experience with C# ,versions 2. • 2+ years of experience with web development including . • Proven knowledge of SQL (versions 2005 -2008) with TSQL. • 2 years of knowledge of a broad range of technologies and practices from different companies."
"מה לא כדאי לכתוב בקורות החיים שלכם? הנה חמישה פרטים שקראתי בלא מעט קורות חיים (כן, כן, כל הכתוב כאן מבוסס על מקרים אמיתיים!) ואפשר בקלות להגדיר אותם כמיותרים/ הורסי שמחות ו...נו, כבר הבנתם את הכוונה... :) :"
מצא פרטים ועוד משרות בלינקדאין-כאן
לחברת אשראי מובילה דרושים מנהלי פרויקטים/מנתחי מערכות.
"דרישות התפקיד: לפחות שנתיים ניסיון בתפקיד מנהל/ת פרויקט בארגון גדול- חובה. ניסיון בניתוח מערכות של שנתיים לפחות-חובה רקע טכנולוגי קודם- חובה. ניסיון והכרות עם שוק ההון (אשראי/בנקאות)-יתרון. קורות חיים מתאימים בלבד יש לשלוח למיכל "
לפרטים הצטרף לקבוצה הגדולה בארץ לחיפוש עבודה
looking for senior software tester (automation+manual)
"Relevant CV's and more info at: "
operation manager from pharmaceuticals arena
"An advanced well established Pharmaceutical/biological SU is seeking for a senior position, reporting to CEO, Operation Manager. 1. Proven capabilities to manage operations ( procurement , production, logistics/ planning ) with Biological products 2. Proven track records in experiencing FDA/ EMEA inspections 3. Proven management capabilities : understanding the big picture and ability to see the details as well. 4. " Executor " in his spirit , hard worker and can make things happen . 5. Ability to work with a small operation group and to groom into additional international operation responsibilities 6. Eduction background in Engineering / Biology / Biochemistry 7. High level of English communication. 8. Previous position as a production manager or production supervisor of a complicatied operational structure 9 Ability to put together an improvements plan - short and long term and assure its execution 10. Team player - ability to work well with its peers Email for CV's : "
"למיזם חדש ומרתק בתחום מדעי החיים, דרוש(ה) מנהל (ת) להקמת מערך השיווק של שירותי החברה, למגזר מוסדי - מדעי שיתרחב, עם הזמן לזרועות נוספות בתחום מדעי החיים. השכלה,רקע וניסיון שיווקי בתחום מדעי החיים - הכרחיים!!! יצירתיות, נמרצות ויכולת להירתם לנושא שבו מאמינים עם כל הנשמה. ייצוגיות, יכולת להציג נושא באופן מדעי ושיווקי, לקהלים מגוונים. אנגלית ברמה גבוהה. Email for CV's : "
a senior r&d manager for a medical device company
"A very interesting Medical Device SU is looking for a Senior R&D manager. Someone with a proven track record in managing R&D operations ( more as a manager of the development activities rather than any research ). Wide knowledge of managing systemic development process and implementing development activities . A methodical type of thinking and hands on management style . - Experience in managing development activities for at least 5-7 years - Background in Biology , Chemistry or Biochemistry (might be an engineer with the above mentioned background). Management experience of a small development team (4-6 people) Reporting to the CEO Email for CV's : "
"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 complian 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 • Good communication skills • Highly organized and detail oriented, with solid analytical and interpersonal skills • Project management skills • Self starter • Ability to effectively handle multiple priorities in a fast paced, action oriented team environment • Accountable, innovate, able to deliver results Email for CV's : "
"לחברת תרופות רב לאומית יוקרתית ,דרושׁ(ה) רופאׁ(ה) לתפקיד של ניהול מערך השיווק של קבוצת תרופות מההיבט המדעי - רפואי, כולל מעורבות במחקרים הקליניים המתנהלים בחברה. בעלי תואר MD ורשיון ישראלי לאחר סטא'ז בארץ תנאים הולמים למועמדים המתאימים רופא(ה) לאחר סטאז' בארץ ובעל(ת) רישיון מוכר בארץ, בראשית הדרך. יכולת להציג פרזנטציות והדרכה לקהלים מגוונים בפורומים שונים. אוריינטציה עסקית אנגלית מעולה. Email for CV's : "
"Reporting and location The VP regulatory affairs will report directly to the CEO - location in the US – NY/NJ/ Responsibility : All regulatory affairs activities in US, Europe and Israel Experience - Proven experience in regulatory affairs related to Biological products including BLA filling - Proven experience in negotiating successful submission within the FDA and EMEA - Experience with wound healing products will be a plus Eduction PHD/MSC in Life sciences preferably Biology or Biochemistry"
looking for software engineer server side send cv to mail
"Looking for Software Engineer • Bachelor's Degree in Computer Science / Software Engineering • Minimum 3 years of Experience in .NET C# • Minimum 2 Experience in SQL – indexing, stored procedures, jobs • Minimum 2 Experience in multi-threaded development Experience in SOA – advantage Experience in Task Parallel Library - advantage • Development environments: -Developing Microsoft Visual Studio -Developing in Windows environment -Programming client/server applications • Experience in WCF • Knowledge of design patterns • High self-learning ability • Independent worker • Good English • Good interpersonal skills"
"Job description: •Developing block and system level verification environments, Bus Functional Models (BFMs), checkers and assertions using verification standard methodologies. •Working in collaboration with the architecture/design/research teams to develop and execute test plans. •Writing directed/random tests and debugging failures. •Writing, analyzing and achieving coverage metrics. •Apply advanced techniques to achieve verification with the highest quality, productivity, and time-to-market Requirements •B.Sc. In EE •Around 1-4 years of experience in ASIC Verification •Experience in verification environments, using SystemVerilog or Specman. •Comfortable with Verilog and industry-standard EDA tools such as NC or VCS •Excellent personal relationships, high motivation, high skills for independent work. "
עוד משרות הייטק בין חברים בלינקדאין
physical design engineer #47271
"•BSc in electronic engineering from any university •At least 4 years of relevant PD experience •2 years Experience in floorplan , P&R using EDI tool from Cadence •Knowledge in scripting languages is a must (TCL preferred) •Good interpersonal relations •Self motivated and problem solver by nature •Knowledge in STA (Static Timing Analysis) is a must (Cadence tools advantage) "
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