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רשימת משרות דרושים רישום / רגולציה בארלוזורוב 83, תל אביב יפו

נמצאו 11 משרות שמתאימות לחיפוש שלך, כולל עבודה במקצועות הבאים: רישום / רגולציה, רוקחות ופארמה,
  • Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: תל אביב-יפו Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1054997 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • עודכן השבוע
    מהנדס /ת איכות ורגולציה (רפואי) שם החברה: QualiGateמיקום המשרה: תל אביב יפו למרכז פיתוח של חברה מובילה דרוש /ה מהנדס /ת איכות ורגולציה מנוסה.
    דרישות:
    - ניסיון קודם בחברות מדיקל כ- Quality Assurance and Regulatory Affairs.
    - תואר אקדמי רלוונטי בתחום המדיקל / ואו QA&RA.
    - ידע ונסיון בעבודה בנאגלית: כתיבה/קריאה/דיבור. המשרה מיועדת לנשים וגברים כאחד.
    הגשת מועמדות פעולות נוספות מס' משרה: 1145721 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 3 ק"מ ממך Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: גבעתיים Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1055007 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 5 ק"מ ממך Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: רמת גן Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1055008 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 8 ק"מ ממך Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: גבעת שמואל Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1055000 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 8 ק"מ ממך Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: חולון Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1055006 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 9 ק"מ ממך מנהל/ת צוות קליני ורגולטורי לחברת סטארט אפ בתחום הרפואי שם החברה: Gal HR - השמה בתחומי המדיקל, הפיננסים ושוק ההון.מיקום המשרה: רמת השרון לחברת סטארט אפ בתחום הרפואי דרוש/ה מנהל/ת צוות קלינית ורגולציה. התפקיד כולל: הובלת התחום הקליני והרגולטורי בחברה, ניהול והובלת הצוות העוסק בתמיכה בצוות הרפואיים בבתי חולים- המבצעים ניסויים קליניים, ניתוח וניהול נתונים, עבודה מול יועצי הרגולציה של החברה- CRO וCRA, עבודה עם תכנת Matlab ועוד.
    *המשרה מיועדת לגברים ונשים כאחד*
    דרישות:
    - בוגר לימודי רפואה, ו / או תואר שני במדעי הרפואה, ביולוגיה.
    - Ph.d – יתרון.
    - ניסיון קודם בליווי ניסויים קליניים מהתחום הרפואי.
    - ניסיון עם CRA ו CRO.
    - ניסיון או הכשרה בתחום הרגולציה הרפואית – יתרון.
    - ניסיון קודם בתפקיד ניהולי- יתרון.
    - הכרה וניסיון עם תוכנת Matlab - יתרון.
    - אוריינטציה ניהולית, יכולות אישיות ובינאישיות גבוהות.
    הגשת מועמדות פעולות נוספות מס' משרה: 1168742 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 9 ק"מ ממך Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: בת ים Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1055005 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 9 ק"מ ממך Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: קריית אונו Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1055004 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 10 ק"מ ממך Regulatory Affairs Specialist שם החברה: טבעמיקום המשרה: אור יהודה Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    דרישות:
    Teva’s Regulatory Affairs team located at Petach Tikva are seeking for a Regulatory Affairs Specialist, who will be responsible for all the supporting activities related to registration and maintenance of Drug Master Files – Electronic submissions, Documents filing, systems update. The role includes:
    Responsibility to prepare and submit the electronic submissions according to industry guidelines
    Proactively collaborates with the Regulatory Associate team members in support activities related to development, registration and maintenance of Drug Master Files, i.e.:
    •Printing and sending DMFs / DL response by hard / soft copy / electronically / eCTD gateway
    •Filling deficiency letters’ response in the SmarTeam/any relevant folder
    Answering customers’ requests asking for LoAs, DMFs, CEPs
    •LoA: Preparation and providing to the relevant MoHs and customers
    •DMFs/CEPs: Sending to the relevant MoHs and customers
    •Deficiency letters responses: Sending to the relevant MoHs and customers and fi
    הגשת מועמדות פעולות נוספות מס' משרה: 1054999 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
  • מיקום: 11 ק"מ ממך מנהל/ת צוות קליני ורגולטורי לחברת סטארט אפ בתחום הרפואי שם החברה: Gal HR - השמה בתחומי המדיקל, הפיננסים ושוק ההון.מיקום המשרה: הרצליה לחברת סטארט אפ בתחום הרפואי דרוש/ה מנהל/ת צוות קלינית ורגולציה. התפקיד כולל: הובלת התחום הקליני והרגולטורי בחברה, ניהול והובלת הצוות העוסק בתמיכה בצוות הרפואיים בבתי חולים- המבצעים ניסויים קליניים, ניתוח וניהול נתונים, עבודה מול יועצי הרגולציה של החברה- CRO וCRA, עבודה עם תכנת Matlab ועוד.
    *המשרה מיועדת לגברים ונשים כאחד*
    דרישות:
    - בוגר לימודי רפואה, ו / או תואר שני במדעי הרפואה, ביולוגיה.
    - Ph.d – יתרון.
    - ניסיון קודם בליווי ניסויים קליניים מהתחום הרפואי.
    - ניסיון עם CRA ו CRO.
    - ניסיון או הכשרה בתחום הרגולציה הרפואית – יתרון.
    - ניסיון קודם בתפקיד ניהולי- יתרון.
    - הכרה וניסיון עם תוכנת Matlab - יתרון.
    - אוריינטציה ניהולית, יכולות אישיות ובינאישיות גבוהות.
    הגשת מועמדות פעולות נוספות מס' משרה: 1168742 קישור למשרהשלח בדוא"ל עוד מהחברהנתקלת בבעיה? שיתוף שלח לחבר
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