R&D Supervisor - Αχαρνές - Kleva Pharmaceuticals

    Kleva Pharmaceuticals
    Kleva Pharmaceuticals Αχαρνές

    πριν 1 εβδομάδα

    Πλήρης απασχόληση
    Περιγραφή

    KLEVA Pharmaceuticals S.A. is a privately owned pharmaceutical and fully integrated company that has been in operation in Greece for over 50 years. Kleva develops and manufactures generic products and focuses on Pharmaceuticals (Rx & OTC).

    Our two manufacturing facilities in the North of Athens, Greece, are equipped with high technology machinery and have the manufacturing potential for a wide range of pharmaceutical forms.

    Our mission is to offer a flexible, fully scalable, qualitative, and cost-effective product development in a wide range of dosage forms. We register and export our products to a number of regulated and non-regulated markets around the world.

    To realize our ambitious goals, KLEVA needs people who are innovators, believe in the values of respect and cooperation and are ready to commit to a company that wants to penetrate new markets, leverage international business development opportunities, and enter contract manufacturing deals.

    How you will support our mission

    We are looking for R&D Supervisor (at Polydendri site)

      Position Summary:

    The R&D Supervisor is part of the Product Development Department, reporting directly to the R&D Manager. This role is responsible for overseeing the analytical R&D laboratory and ensuring the effective development and evaluation of generic pharmaceutical products.

    Main Responsibilities

    • Supervise the Analytical R&D Laboratory in the development of generic pharmaceutical products.
    • Monitor laboratory equipment and instruments to minimize downtime and reduce maintenance costs.
    • Provide technical support, including (but not limited to) drafting and reviewing analytical method validation/verification protocols and reports.
    • Evaluate analytical results generated by the laboratory.
    • Perform troubleshooting of laboratory equipment and instruments.
    • Communicate effectively with clients and internal teams, providing analytical information and data for ongoing projects.
    • Draft and organize the daily analytical schedule of the laboratory in collaboration with the R&D Manager.
    • Liaise with suppliers and service providers regarding R&D laboratory equipment.
    • Oversee the training, development, and performance of R&D laboratory team members.

    Candidate Profile & Key Qualifications

    Academic Background

    • Bachelor's degree in Life Sciences, preferably in Chemistry

    Languages:

    • Fluency in English both written and oral

    Special Knowledge

    • Excellent computer literacy (MS Office)

    Qualifications 

    • Minimum of four (4) years of professional experience in R&D pharmaceutical analysis.
    • Proven experience in analytical method validation and verification.
    • Strong multitasking and time-management skills.
    • Ability to work effectively under tight deadlines.
    • Up-to-date knowledge of EU guidelines on pharmaceutical development requirements.

     Benefits

    • Work in a friendly and challenging environment
    • Competitive salary
    • Private insurance
    • Personal development opportunitie

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