משרות נוספות בתחום: עובד רגולציה , עוזר רגולציה
Regulatory Affairs Specialist II
  • תל אביב - יפו
  • משרה מלאה
  • לא צוין שכר
תיאור המשרה:
Prepare and maintain electronic submissions (eCTD) of DMFs, via a publishing system, according to industry guidelines.
Submission of DMFs, prepared by RA team, to authorities according to relevant guidelines.
Routine support and collaboration with the Regulatory Affairs Associates team members in administrative activities related to submissions and technical preparation of DMFs.
Answering and supporting customers’ requests by providing administrative information (DMFs, CEPs, Deficiency letters responses prepared by RA team) and additional categories as needed, via CRM.
Filling RA documents in CRM and Smarteam systems.
Distribution of costumer notifications prepared by RA team via the CRM system.
Learning of submission regulatory guidance and internal work processes
Working with several submission systems in parallel and different gateways according to authority’s requirements.
דרישות המשרה:
Capabilities:
Good human communications
High service approach to internal & external customers
The ability to adapt to new ways of working and learn new processes.
Organized
Technical skills
Individual work ability as well as teamwork
Meeting work target timelines
Readiness to work when required
Ability for self-learning
Initiative
Self-motivated
Time management
English - good professional level, both in writing and speaking
Former experience working in a pharma company/regulation (advantage)
מעבר למשרות דומות בתחומים:
משרה מספר 9114703
metapel
על החברה:
טבע תעשיות פרמצבטיות
גודל חברה: 1001-5000
תעשייה: תרופות
טבע תעשיות פרמצבטיות בע"מ
המשרות באתר מיועדות לנשים וגברים כאחד