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טבע תעשיות פרמצבטיות

    דרושים טבע תעשיות פרמצבטיות

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    משרות טבע תעשיות פרמצבטיות

    הצעות עבודה
    מתוך 1
    נמצאו 3 משרות
    1 ימים
    טבע תעשיות פרמצבטיות
    Location: Shoham
    Job Type: More than one
    Teva Pharmaceuticals Industries Located in Shoam is looking for a quality analyst for temporary position.
    Job Purpose:
    Ensure that quality complaints are registered, investigated, periodically monitored and adequate corrective actions are taken.
    Responsible for batch review and final release for medical devices, cosmetics and food supplements products.
    Responsible for quality approval and management of suppliers/ manufacturers.
    Supporting QA Compliance activities.
    Requirements:
    Appropriate knowledge in Pharmaceutical Science, Business, Healthcare or an equivalent combination of education and experience to the functional role.
    Minimum of 1 year of experience in Quality Assurance within the pharmaceutical industries considered as advantage.
    Proficient computer skills in current software including MS office
    Fluent English.
     
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    5999686
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    עדכון קורות החיים
    לפני שליחה
    1 ימים
    טבע תעשיות פרמצבטיות
    Location: Netanya
    Job Type: Full Time and English Speakers
    Ensures data management activities and deliverables for area(s) of responsibility are completed in line with business requirements and company objectives.
    Evaluates and approves service level agreements.
    Oversees service providers to perform core data management functions including CRF, edit check development, eCOA, user acceptance testing, data cleaning, reviewing listings, and database locking procedures.
    Evaluates and makes recommendations related to inter- and intra-departmental processes in order to identify and implement efficiencies and quality improvement measures.
    Requirements:
    Managers require at least five years (Senior Managers seven years) of data management experience in a pharmaceutical or clinical research setting.
    Bachelors Degree or higher, or equivalent amount of combined educational and work experience is required.
    Exceptional candidates may be considered with less years depending on experience and education.
    Experience in data management, systems, technical and outsourcing.
    Understanding of FDA and international regulations and GCP.
    Experience with computerized clinical data management systems.
    Thorough understanding of the drug development process, clinical trial methodology, GCP regulations, and data management principles.
    Strong understanding and experience with eCOA and ePRO systems and leading stuides with eCOA.
    Strong and effective oral and written communication skills and interpersonal skills.
     
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    6038760
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    עדכון קורות החיים
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    לפני 23 שעות
    טבע תעשיות פרמצבטיות
    Location: Tel Aviv-Yafo
    Job Type: Full Time and Temporary
    To lead and proactively manage all regulatory activities associated with development, registration and maintenance of Drug Master Files according to current international regulatory requirements.
    The position is temporary for 6 months, with the option to extend permanently.
    Requirements:
    Master degree in relevant field, e.g. chemistry/biochemistry/biology or biotechnology - must.
    PhD in relevant field - advantage.
    Good communication skills, high service approach to internal & external customers.
    Good Leadership and communication skills.
    Self- learning capabilities.
    Independence.
    Organized.
    High level writing skills.
    Comprehensive work.
    Time management and meeting work target time lines abilities.
    Accuracy.
    Self-motivated and initiative.
    Good professional English level, both in writing and speaking.
     
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    6097628
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    עדכון קורות החיים
    לפני שליחה
    מתוך 1

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