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Join Us

Medinol is a well-established and renowned industry-leading company built around a team of passionate professionals. We embrace personal and professional growth, thrive on out-of-the-box thinking, reward excellence, and take pride in creativity. Our people believe that through our dedication to helping each other and the community in which we live, we ultimately enrich ourselves, too. In a very real sense, Medinol is a family.

If you are a talented team player and a highly-motivated, focused and energetic individual who wants to make an impact, we would love to hear from you.

Job Opportunities

  • Regulatory Project Leader - Regulatory, Jerusalem

    Job Description

    • Prepare and manage various submissions and correspondence to regulatory authorities ensuring adherence to national and international regulations and standards (e.g. FDA, Health Canada, European Union and Asia)
    • Coordinate the regulatory aspects of the product approval process
    • Support and provide regulatory input for different R&D and manufacturing activities
    • Support regulatory compliance activities for post market vigilance reporting

    Job Requirements

    • Bachelor’s degree in a Science discipline is required – life science, biochemistry, pharmacy or chemistry preferred
    • A minimum of 5 years experience in regulatory affairs in a medical device/pharmaceutical drug development company
    • Demonstrable experience in successfully developing and managing regulatory submissions
    • Prior experience with preparation of CMC sections for regulatory submissions, as well as experience in registration of Device-Drug Combination Products (Class III) is highly desirable
    • Knowledgeable in FDA, EU, and/or Global regulatory submission processes
    • Exceptional organizational skills, ability to multi-task and be detail oriented
    • Ability to work well under pressure / Time management skills
    • English – mother tongue level/high proficiency
    Apply Now
    CV

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  • Complaint Coordinator - QS, Jerusalem

    Job Description

    • Ensure that all complaints are acknowledged and completed in a given timeframe
    • Identify complaints that require escalation as a potential reportable event based on established criterion and applicable regulations and notify accordingly management
    • Create required reports, ensuring they are prepared and approved according to internal procedures and that the reports are maintained as part of the complaint file
    • Communicate and interact cross-functionally on a regular basis regarding Customer Complaints
    • Prepare periodic reports relating to complaints, product problems, etc.
    • Support other tasks in Quality System as assigned

    Job Requirements

    • Bachelor’s degree in a Science discipline is required
    • Experience in the medical device industry – Advantage
    • Experience handling customer complaints – Advantage
    • Hands-on approach mentality
    • Excellent computer and presentation skills
    • Strong organizational and time management skills
    • Ability to work independently and amongst a team with minimal supervision
    • High attention to detail and ability to solve problems and communicate issues
    • Ability to work on multiple projects simultaneously
    • Ability to review, analyze, summarize, and interpret data; draw conclusions and make appropriate recommendations and decisions; write reports.
    • Willingness to work full-time in Jerusalem
    Apply Now
    CV

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  • Document Editor - Regulatory, Tel Aviv

    Job Description

    We are currently looking for a talented Document Editor that will review regulatory submissions and clinical documents (protocols, clinical studies sumaries, etc.) for accuracy, completeness, and usefulness, or fitness of purpose.

    • Read content and correct for errors in spelling, punctuation, and grammar
    • Rewrite copy, as needed, to make it easier for people to understand
    • Verify facts, using standard reference sources
    • Evaluate submissions and decide what to publish
    • Work with scientific content writers to help their documents succeed
    • Plan documents in accordance with the organization’s style and content policies
    • Develop content ideas while being mindful of the target audience (e.g., health ministries)
    • Allocate space for text, photos, and illustrations that help convey the document’s meaning
    • Approve final versions of documents submitted by staff
    • Supervise document development cycle
    • Develop documents templates

    Job Requirements

    • A bachelor’s degree in English, journalism, or communications is required
    • 2 years or more of business/technical writing experience
    • English – mother tongue level/proficient (High level writing skills)
    • Experience with document editing, document management, and publishing software (e.g., Microsoft Word, PowerPoint, PDF software) is a must.
    • Excellent communication skills
    • Ability to work well with people at every level of the organization
    Apply Now
    CV

    Doc, Docx, PDF