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מיקום נוכחי: לא ניתן לזהות את מיקומך לצפייה בסרטון הסבר

טבע

אודות החברה:

טבע, שהוקמה בשנת 1901, מדורגת כיום בין 10 חברות התרופות המובילות בעולם. טבע, שמשרדה הראשי נמצא בישראל, פעילה ב-60 מדינות ומעסיקה למעלה מ-46,400 עובדים מסורים ברחבי העולם.

כחברת תרופות עולמית עם הפנים לעתיד, עומדת חברת טבע בראש הפיתוח, הייצור והשיווק של מגוון רחב של תרופות ייעודיות, תרופות גנריות, תרופות ללא מרשם, חומרים פעילים לתעשייה הפרמצבטית (API) ותכשירים טיפוליים חדשניים.

בכל צעד שלנו אנו מתנהלים בהתאם לערכים המנחים אותנו: יושרה, כבוד, שיתוף פעולה, מצוינות ומובילות. הערכים הללו מגלמים את האופי שעל פיו פועלת טבע. הם מאפשרים לנו להביא לעולם תרופות בטוחות ויעילות באמצעות איכות העובדים והמוצרים שלנו. ערכים אלה נמצאים בבסיס המחויבות שלנו לחולים, והמסירות הבלתי פוסקת שלנו לחולל שינוי משמעותי.
מס' עובדים: מעל ל-5000
מס' משרות: 85
  • מנהל/ת משאבי אנוש באתר טבע-טק שם החברה: טבעמיקום המשרה: באר שבע תחומי אחריות עיקריים:
    1.שותפה לקביעת יעדים ותכניות עבודה למערך HR של טבעטק בהתאם ליעדי העסק.
    2.תמיכה מלאה במנהלים איתם עובדת
    3.ליווי היישום וההטמעה של שינויים ארגוניים בעסק.
    4.ייעוץ, הנחיה ותמיכה מקצועית למנהלי היחידות
    5.אחריות ניהולית ומקצועית בתחומים הבאים: מיון, גיוס וקליטת עובדים, הדרכה מקצועית של עובדים, תהליכי פיתוח ארגוני ופיתוח מנהלים, תהליכי הערכת עובדים וביצוע, שכר, כלכלת עבודה, רווחה, תרבות ופנאי, שימור עובדים.
    6.ניהול HR בהלימה ל: Compliance ולמדיניות החברה
    7.העבודה במשרה מלאה באתר החברה בנאות חובב
    דרישות:
    השכלה – תואר אקדמי מדעי ההתנהגות/ מדעי החברה/ משאבי אנוש
    ניסיון- לפחות 5 שנות ניסיון כמנהלת מש"א
    כישורים – ראייה מערכתית, יחסי אנוש טובים, שירותיות, יכולת עמידה בלחץ, עבודת צוות
    מס' משרה: 877648 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: בת ים Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867108 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: בת ים The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867119 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Marketing Manager שם החברה: טבעמיקום המשרה: רמלה Teva’s commercial IL unit is hiring a marketing manager for a unique group combining marketing of medical devices and dru .g
    The job includes:
    Building unit marketing advantages based on deep scientific understanding of various product lines (marketing manager will be responsible for both scientific research gathering and processing)
    Developing marketing material and supporting business product managers including direct support and interaction with customers
    Developing and managing 3rd party scientific studies to support business marketing advantage
    Leading and developing groups of key opinion leaders on ongoing products and introducing future products in cooperation with unit medical director
    דרישות:
    Phd in life sciences/pharmacy/chemistry - must
    Previous experience in the pharmaceutical/medical device industry - mandatory
    Previous experience in working with and presenting to hospital/ medical staff- must
    Previous experience in Regulatory affairs- an advantage
    Previous experience in a scientific management position – advantage
    מס' משרה: 843803 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • אח/ות שם החברה: טבעמיקום המשרה: רמלה טבע מגייסת אח/ות מוסמכ/ת למוצר ייחודי ,
    במסגרת התפקיד:
    שימור ותמיכה בחולים תחת הטיפול, העלאת ההיענות והדבקות בטיפול.
    ביצוע הדרכות למטופלים חדשים ורענון הדרכות למטופלים קיימים.
    תיעוד ממוחשב של המידע הרלבנטי.
    ביצוע ביקורי בית אצל המטופלים.
    שליטה מקצועית בחומר הנדרש.
    ניהול קשר שוטף עם הצוות הרפואי בכל הנוגע לטיפול בחולה.
    אחריות אדמיניסטרטיבית בכל הקשור להמשך תקין ושוטף בטיפול.
    דרישות:
    אח/ות מוסמכ/ת - חובה
    כשלוש שנות ניסיון כאח/ות מוסמכ/ת מבתי חולים או בקהילה – חובה
    הכרות עם תוכנות office
    אנגלית ברמה גבוהה מאוד
    זמינות לעבודת שטח במשרה מלאה
    נכונות לנסיעות בכל הארץ
    מס' משרה: 827839 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: חולון Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867109 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: חולון The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867120 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Marketing Manager שם החברה: טבעמיקום המשרה: לוד Teva’s commercial IL unit is hiring a marketing manager for a unique group combining marketing of medical devices and dru .g
    The job includes:
    Building unit marketing advantages based on deep scientific understanding of various product lines (marketing manager will be responsible for both scientific research gathering and processing)
    Developing marketing material and supporting business product managers including direct support and interaction with customers
    Developing and managing 3rd party scientific studies to support business marketing advantage
    Leading and developing groups of key opinion leaders on ongoing products and introducing future products in cooperation with unit medical director
    דרישות:
    Phd in life sciences/pharmacy/chemistry - must
    Previous experience in the pharmaceutical/medical device industry - mandatory
    Previous experience in working with and presenting to hospital/ medical staff- must
    Previous experience in Regulatory affairs- an advantage
    Previous experience in a scientific management position – advantage
    מס' משרה: 843802 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • אח/ות שם החברה: טבעמיקום המשרה: לוד טבע מגייסת אח/ות מוסמכ/ת למוצר ייחודי ,
    במסגרת התפקיד:
    שימור ותמיכה בחולים תחת הטיפול, העלאת ההיענות והדבקות בטיפול.
    ביצוע הדרכות למטופלים חדשים ורענון הדרכות למטופלים קיימים.
    תיעוד ממוחשב של המידע הרלבנטי.
    ביצוע ביקורי בית אצל המטופלים.
    שליטה מקצועית בחומר הנדרש.
    ניהול קשר שוטף עם הצוות הרפואי בכל הנוגע לטיפול בחולה.
    אחריות אדמיניסטרטיבית בכל הקשור להמשך תקין ושוטף בטיפול.
    דרישות:
    אח/ות מוסמכ/ת - חובה
    כשלוש שנות ניסיון כאח/ות מוסמכ/ת מבתי חולים או בקהילה – חובה
    הכרות עם תוכנות office
    אנגלית ברמה גבוהה מאוד
    זמינות לעבודת שטח במשרה מלאה
    נכונות לנסיעות בכל הארץ
    מס' משרה: 827838 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: תל אביב-יפו Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867101 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: תל אביב-יפו The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867112 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: גבעתיים Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867110 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: גבעתיים The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867121 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: אור יהודה Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867103 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: אור יהודה The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867114 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: רמת גן Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867111 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: רמת גן The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867122 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: יהוד-מונוסון Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867106 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: יהוד-מונוסון The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867117 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Procurement Service Center Team Lead 5581 שם החברה: טבעמיקום המשרה: קריית אונו Teva Pharmaceuticals Located in Petach Tikva is seeking a Procurement Service Center Team
    The Procurement Service Center Team Lead is responsible to act as liaison between the Procurement Service Center (PSC) and Stakeholders to ensure relationships and processes between the Procurement Service Specialists and the internal customers are effectively managed within the agreed upon SLAs and supports continuous improvement and integration initiatives The PSC Team Lead will also be responsible for overseeing the activities of Procurement Service Specialists for direct and/or indirect operational and tactical Procurement activities based on established policies and practices. He/She is responsible to ensure Service Specialist team’ targets and KPIs are met and/or exceeded.
    Essential Duties & Responsibilities: Ensure delivery of high quality service to internal clients and suppliers where applicable. Support the implementation of improvement and integration initiatives and ensure efficient
    דרישות:
    Bachelors degree or equivalent experience in Finance, Supply Chain or related business area
    Minimum of 3 years of procurement operations/transaction experience.
    Minimum of 3 years in a supervisory position
    Proficiency of English (written/verbal), Strong ability to influence others
    Specialized or Technical Knowledge Licenses
    six Sigma certification preferred
    Procurement transaction management, Procure to Pay processes and tools (incl. Ariba)
    Shared Services experience and experienced in continuous improvement tools & processes.
    Indirect & Direct Procurement
    Travel between facilities within North America , IL and European countries. Approximately 5%
    מס' משרה: 867107 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: קריית אונו The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867118 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: גבעת שמואל The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867115 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: גני תקווה The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867116 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Marketing Manager שם החברה: טבעמיקום המשרה: שוהם Teva’s commercial IL unit is hiring a marketing manager for a unique group combining marketing of medical devices and dru .g
    The job includes:
    Building unit marketing advantages based on deep scientific understanding of various product lines (marketing manager will be responsible for both scientific research gathering and processing)
    Developing marketing material and supporting business product managers including direct support and interaction with customers
    Developing and managing 3rd party scientific studies to support business marketing advantage
    Leading and developing groups of key opinion leaders on ongoing products and introducing future products in cooperation with unit medical director
    דרישות:
    Phd in life sciences/pharmacy/chemistry - must
    Previous experience in the pharmaceutical/medical device industry - mandatory
    Previous experience in working with and presenting to hospital/ medical staff- must
    Previous experience in Regulatory affairs- an advantage
    Previous experience in a scientific management position – advantage
    מס' משרה: 843804 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • אח/ות שם החברה: טבעמיקום המשרה: שוהם טבע מגייסת אח/ות מוסמכ/ת למוצר ייחודי ,
    במסגרת התפקיד:
    שימור ותמיכה בחולים תחת הטיפול, העלאת ההיענות והדבקות בטיפול.
    ביצוע הדרכות למטופלים חדשים ורענון הדרכות למטופלים קיימים.
    תיעוד ממוחשב של המידע הרלבנטי.
    ביצוע ביקורי בית אצל המטופלים.
    שליטה מקצועית בחומר הנדרש.
    ניהול קשר שוטף עם הצוות הרפואי בכל הנוגע לטיפול בחולה.
    אחריות אדמיניסטרטיבית בכל הקשור להמשך תקין ושוטף בטיפול.
    דרישות:
    אח/ות מוסמכ/ת - חובה
    כשלוש שנות ניסיון כאח/ות מוסמכ/ת מבתי חולים או בקהילה – חובה
    הכרות עם תוכנות office
    אנגלית ברמה גבוהה מאוד
    זמינות לעבודת שטח במשרה מלאה
    נכונות לנסיעות בכל הארץ
    מס' משרה: 827840 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Global sales and operations supply leader 10261 שם החברה: טבעמיקום המשרה: פתח תקווה The position includes the following responsibilities:
    •Coordinating all facets of the S&OP process to provide an optimum customer Service level and working capital performance as defined by the organization’s business operating plans and strategic objectives.
    •partnering with the marketing and sales, to ensure the demand consensus process delivers an agreed upon, workable volume forecast, identifying incremental demand, Ensuring gaps and overlaps are addressed, scenarios are completed and issues appropriately escalated to meet business objectives
    •working closely with other key functions, including Finance, Purchasing, Customer Services, Marketing, Sales and Operation to ensure that the appropriate data is available and accurate to be reviewed at the S&OP process meetings
    •lead and facilitate the S&OP management reviews with senior Leadership and sites GM’s, organize the participation of key people, prepare all data and metrics for review, identify critical issues, gaps and scenarios
    דרישות:
    B.Sc Industrial Engineering and Management/ Bio- technology/ Chemical engineering- must
    At least 3-6 years in Supply chain areas- must
    experience from Pharmaceutical/ food industry- must
    Proven leadership skills in a matrix environment
    Very strong analytical skills
    Excellent interpersonal and communication skills
    Organized and efficient, capable to perform well with multiple priorities and interfaces and constructively challenge stakeholders
    Customer-oriented pro-active attitude: takes initiative, creates an achievement environment
    Process-oriented mind-set to manage complexity and changes
    ability to work in a global environment
    מס' משרה: 867113 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Legal Intern (8466) שם החברה: טבעמיקום המשרה: פתח תקווה למחלקה משפטית של חברת טבע, דרוש/ה מתמחה למועד מרץ 2019.
    תחומי העיסוק העיקריים של המתמחה הם ליווי משפטי שוטף של היחידות העסקיות של החברה בתחום אזרחי/מסחרי.
    התפקיד כולל:
    1.הכנת חוזים והסכמי סודיות.
    2.השתתפות בניהול משא ומתן המתנהל במסגרת פגישות.
    3.מתן מענה לשאילתות ובדיקת סוגיות בהסכמים קיימים.
    המשרה במשרדי החברה בפתח תקווה.
    דרישות:
    * בוגר תואר משפטים.
    * אנגלית ברמה גבוהה מאד, הכוללת יכולת ניסוח בכתב.
    * יכולת וורבלית גבוהה.
    מס' משרה: 867123 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: רמת השרון •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856106 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: רמת השרון Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840183 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: רמת השרון A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821030 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: הרצליה •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856105 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: הרצליה Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840182 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: הרצליה A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821029 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: הוד השרון •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856111 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: הוד השרון Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840188 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: הוד השרון A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821035 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: ראש העין •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856110 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: ראש העין Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840187 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: ראש העין A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821034 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: רעננה •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856113 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: רעננה Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840190 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: רעננה A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821037 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: כפר סבא •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856112 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • טכנולוג/ית לגרנולציה (6111) שם החברה: טבעמיקום המשרה: כפר סבא לאתר טבע בכפר סבא דרוש/ה טכנולוג/ית לתפקיד מאתגר הכולל:
    קליטת תהליכים וטכנולוגיות חדשות בתחום.
    ייזום שיפורים תהליכיים והנדסיים וטיפול בבעיות במערכות, תהליכים וציוד.
    כתיבת ואישור מסמכי יצור כגון הוראות עבודה, נהלי עבודה ושיטות ייצור.
    קיום ממשק עבודה קבוע עם מחלקות האחזקה, מו"פ, מעבדה, הנדסה, MS&T ועוד.
    פתיחה ועריכה של בקרות שינוי.
    טיפול בתקלות ואירועים חריגים בתחום לרבות תיעוד, בקרה ודיווח.
    ביצוע תחקירים והטמעת פעולות מונעות ומתקנות.
    ניהול מעקב תהליכי (לרבות איכות, ניצולת וקיבולת).
    הרצת ציוד חדש בתחום.
    ביצוע הדרכה לצוות התחום.
    השתלבות בצוותי שיפור והרצה מפעליים.
    הכנת המחלקה והשתתפות בביקורות חיצוניות ופנימיות.
    דרישות:
    תואר בהנדסת כימיה/ מכונות- חובה.
    ניסיון של שנתיים לפחות בתהליכי ייצור- חובה.
    הכרות עם עולם ה Lean Management - יתרון.
    הבנה טכנית.
    יכולת ביטוי בע"פ ובכתב ברמה גבוהה (עברית ואנגלית).
    מס' משרה: 853063 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: כפר סבא Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840189 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: כפר סבא A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821036 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • ראש צוות מעבדת QC (6703) שם החברה: טבעמיקום המשרה: כפר סבא לאתר טבע בכפר סבא דרוש/ה ראש צוות למעבדת QC . במסגרת התפקיד:
    ניהול ישיר של צוות אנליטיקאים (כ10 עובדים)
    אחריות לבניה וניהול תוכניות עבודה
    פיתוח עובדים, הסמכות, תוכניות התייעלות
    ניהול תחקירי מעבדה
    הכנה וליווי ביקורות איכות
    דרישות:
    תואר ראשון רלוונטי במדעי החיים/רוקחות/כימיה/הנדסת כימיה/ביולוגיה/ביוטכנולוגיה - חובה.
    ניסיון קודם בטכנולוגיות כרומטוגרפיות (HPLC, GC), שיטות ספקטרוסקופיות (UV, FTIR), טיטרציות וכימיה רטובה.
    ניסיון ניהולי של שנה לפחות - חובה.
    אנגלית – ברמה טובה.
    כושר עמידה בריבוי משימות ועבודה מול ממשקים מרובים.
    כושר הובלה ויחסי אנוש טובים.
    מס' משרה: 843808 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • מנהל/ת מעבדת QC (7421) שם החברה: טבעמיקום המשרה: כפר סבא לאתר טבע בכפר סבא דרוש/ה מנהל/ת למעבדת QC. במסגרת התפקיד:
    ניהול הפעילות הכוללת במעבדה לרבות ניהול ראשי צוותים .
    בניית תוכנית עבודה והגדרת יעדים ויישומם.
    אחריות לעמידה בתפוקות ושמירה על איכות במעבדה.
    עבודה בסביבת full GMP תוך הקפדה על כל הדרישות של Data Integrity
    פתרון בעיות מקצועיות.
    יישום והטמעת טכנולוגיות מתקדמות במעבדה.
    הוצאה לפועל של פרויקטים.
    קשר רצוף עם גורמים בארץ ובחו"ל.
    קבלת החלטות בתחום בקרת האיכות.
    דרישות:
    תואר ראשון בתחומי מדעי החיים - חובה
    תואר שני - יתרון משמעותי
    חמש שנות ניסיון לפחות בניהול מעבדה - חובה
    ניסיון בניהול עובדים - חובה
    אנגלית ברמה טובה מאוד - חובה
    נכונות לשעות נוספות
    מס' משרה: 843815 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: נתניה •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856107 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: נתניה Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840184 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: נתניה A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821031 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Regulatory Affairs International Markets Team Member-8295 שם החברה: טבעמיקום המשרה: נתניה Teva’s Regulatory Affairs (RA) unit is hiring an RA person to lead and proactively manage all regulatory activities associated with development, registration and maintenance of Specialty products in different markets.
    Main Responsibilities:
    Accountable for the development and implementation of regulatory strategies in the International Markets (IM) region
    End-to-end leader of the registration process in IM countries
    Represent IM RA in global regulatory teams
    Assessment of business development opportunities from an IM regulatory perspective
    דרישות:
    • BSc/MSc in chemistry/biology/biotechnology/pharmacy or similar scientific field
    • Experience in regulatory affairs for pharmaceuticals/biologics
    • Basic familiarity with submission routes of NCE/biologics to major Health Authorities (EMA and FDA) – Advantage
    • Familiarity with CTD format and ICH requirements for registration of pharmaceuticals/biologics/devices – Advantage
    • Good leadership, project management and communication skills
    • Self-learning & Multi-tasking capabilities
    • Excellent spoken and written English is essential
    • Proficiency in other languages - advantage
    מס' משרה: 843812 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: חדרה •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856109 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: חדרה Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840186 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: חדרה A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821033 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Manager, Global Clinical Project Management ׁ(9794) שם החברה: טבעמיקום המשרה: זכרון יעקב •Oversee the development of the operational plans for clinical deliverables for assigned studies, effectively implementing design excellence in line with the study protocol and ensuring the principles of GCP.
    •Collaborate with CQA to establish a study auditing plan to ensure timely resolution of CQA audit findings at the global study and collaborate with Inspection readiness to ensure study is ready for inspection (if applicable).
    •Accountable for the performance and results of global studies, including:?Foster a collaborative, innovative, problems-solving culture with cross-functional team members for timely and high quality execution of studies.
    ?Manage the third party vendors working closely with Procurement for performance and quality metrics.
    ?Conduct and/or ensure completion of all oversight activities (e.g. oversight site visits, monitoring report review) as per the study vendor management plan.
    ?Ensure the appropriate information is communicated to management including but not
    דרישות:
    •Undergraduate/BSc degree or higher in applicable discipline and a minimum of 5 years of related experience.
    •At least 4 years of experience pharmaceutical industry or clinical research site based experience.
    •Knowledge of GCP guidelines.
    •Computer literate.
    •Fluent in English.
    •Global trial experience preferred.
    •Monitoring experience preferred.
    •Must be able to travel with overnight stays, as necessary, travel up to 30%.
    מס' משרה: 856108 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Pharmacology Researcher (9679) שם החברה: טבעמיקום המשרה: זכרון יעקב Teva is seeking candidates to fill a full-time position as an a expert in the field of pre-clinical pharmacology at the R&D site in Netanya (Abic)
    We are seeking for an experienced scientist (M.Sc, PhD) to join the pharmacology department. The successful candidate will perform research for drug development in the pharmaceutical industry.
    Main focus will be investigating the efficacy and mode of action of novel drug therapies in animal models
    The position requires experience in the conduct of in vivo disease models using endpoints with high translational relevance.
    The candidate should have knowledge of disease biology and molecular targets in one or more of the following therapeutic areas: Pain, autoimmune disorders, respiratory indications and oncology.
    Expertise in laboratory animal science, surgical procedures, veterinary medicine, and animal care are an advantage.
    Duties and responsibilities:
    1.Design, perform and support experiments in the field of expertise.
    2.Planning and ex
    דרישות:
    M.Sc, /PhD/ level
    •experience in the conduct of in vivo disease models
    •Expert knowledge of pharmacological models "hands on" experience in set up and conduct of test systems
    •Strong interpersonal skills
    •Excellent English (oral , written)
    •Industry experience, R&D focus areas highly desired, development of biological products is an advantage
    מס' משרה: 840185 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • Senior Medical Writer (9118) שם החברה: טבעמיקום המשרה: זכרון יעקב A Senior Medical Writer, in Global Regulatory Medical Writing, provides intermediate medical writing support to Clinical Specialty Development (and other departments as appropriate) in the production of clinical research documentation in support of drug development, product registrations, and product marketing.
    Essential Functions:
    •Writes and/or edits clinical regulatory documents (generally clinical study protocols/amendments, clinical study reports, and Investigator’s Brochures and briefing documents)
    •Ensures that these documents are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
    •Prepares other documents for regulatory submissions
    • Advises Clinical (and other) staff on the organization and presentation of information within documents, as well as the design and format of data displays.
    •Ensures quality assurance of own documents
    •Provides leadership/strategy at the cross-functional study-team level for individual do
    דרישות:
    •PhD/PharmD in life sciences (or other related field) with a minimum of 2 years of experience related to medical writing, Masters in life sciences (or other related field) with a minimum of 3 years of experience or Bachelor’s degree with a minimum of 5 years of experience.
    •Excellent English, both written and spoken.
    •Intermediate writing and editing skills and competence in the use of relevant software applications, and using templates, and other electronic formats
    •Intermediate knowledge of government regulations pertaining to drug development and understanding of the Company’s products and standard operating procedures (SOPs)
    •Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
    •Good organizational/planning and problem-solving skills at the document level
    •Excellent presentation and written communication skills
    •Works successfully with an intermittent level of direct supervision
    מס' משרה: 821032 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • מפעיל/ת מכונה לאתר בקריית שמונה-4058 שם החברה: טבעמיקום המשרה: קריית שמונה לאתר טבע בקרית שמונה דרוש/ה מפעיל/ת מכונה לתפקיד הכולל:
    הפעלת מכונות ייצור ואריזה, ביצוע Set-Up, תיקון תקלות ואחזקה מונעת
    בקרת איכות על פעולות המכונות, עבודה עם מערכות ממוחשבות
    דרישות:
    ידע טכני נרחב ומוכח בהפעלת מכונות בתעשייה - חובה
    הנדסאי/ת מכונות - יתרון משמעותי
    אנגלית בסיסית - חובה
    ראייה מערכתית ועבודה בצוות
    נכונות לעבודה בשלוש משמרות ושעות נוספות, לרבות ימי שישי בבוקר ומוצאי שבת על פי צורכי המערכת
    מס' משרה: 843813 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
  • עובד/ת ייצור לאתר קרית שמונה-7589 שם החברה: טבעמיקום המשרה: קריית שמונה לאתר טבע בקרית שמונה דרוש/ה עובד/ת ייצור לתפקיד הכולל:
    עבודת הרכבות ידניות, עבודה עם ממיסים, מילוי טפסים, בקרה עצמית
    תשומת לב מרבית לאיכות המוצר
    עבודה מאומצת הדורשת ביצוע פעולות החוזרות על עצמן בזריזות וריכוז רב
    דרישות:
    ניסיון בתפקיד דומה- יתרון משמעותי
    ראייה מערכתית ועבודה בצוות
    עבודה בשלוש משמרות וכן שעות נוספות רבות, לרבות ימי שישי ומוצ"ש על פי צורכי המערכת
    משרה מלאה במפעלנו בקרית שמונה
    המשרה מתאימה גם לעבודה מועדפת
    מס' משרה: 843814 הגשת מועמדות פעולות נוספות קישור למשרהשלח בדוא"ל נתקלת בבעיה? שיתוף שלח לחבר
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