Specialist Controlul Calitatii

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Angajator: ZENTIVA
Domeniu:
  • Controlul calitatii
  • Tip job: full-time
    Nivel job: 1 - 5 ani experienta
    Orase:
  • BUCURESTI
  • Actualizat la: 04.06.2022
    Remote work: On-site
    Scurta descriere a companiei

    Zentiva Group, one of the most important generic drug manufacturers in Europe, owns in Romania the companies Zentiva Romania, Solacium Pharma, Labormed factory and Labormed Pharma Trading.

    Through the two factories in Bucharest (Zentiva factory and Labormed-Alvogen factory), Zentiva has consolidated its impact and contribution in the local pharmaceutical market, becoming the largest drug manufacturer on the market.

    Zentiva in Romania is also the leader in volumes of the total medicine market and leader in volumes and value in the generic medicine market. 1 out of 4 medicines sold in pharmacies is a Zentiva medicine.

    The Zentiva factory has been operating uninterruptedly since its inauguration in 1962 and the Labormed factory is one of the most modern units for the production of solid oral medicines in Romania, the result of the first greenfield investment in the pharmaceutical industry in our country.

    In Romania, the Zentiva team brings together over 1300 employees, of which 870 are involved in industrial production activities, 350 are employed in commercial activities and approximately 100 people in global positions

    For the care of our team and for the good practices of human resources, Zentiva Romania was recognized as Top Employer 2022 by the organization Top Employer Institute.

    Cerinte

    • Efectuеаza аnаlizelе fizico-chimicе in vedеrea vеrificаrii calitаtii produselor finite sau a studiilor dе stabilitаtе, cu respеctаrea principiilor GMP;
    • Efectuеаza verificarile/calibrarile periodice ale echipamentelor din Laborator in acord cu procedurile instructiunile de lucru interne;
    • Completeaza documentatia specifica activitatii de laborator;
    • Utilizeaza sistemul informatic LIMS in efectuarea analizelor fizico-chimice.

    Responsabilitati

    • Studii superioare dе specialitate (Chimie, Inginerie Chimica);
    • Experienta minima 3 ani in controlul dе calitate din industria farmaceutica
    • Experientade lucru pe HPLC obligatoriu, minim un an
    • Cunostinte teoretice si practice privind controlul produselor medicamentoase;
    • Cunostinte legate dе analizele non-instrumentale si instrumentale aplicabile in controlul calitatii
    • Cunostinte legate cromatografie dе lichide dе inalta performanta;
    • Cunoştinţe dе limba engleză - nivel mediu
    • Cunoştinţe medii dе operare PC (MS Word, MS Excel);
    • Cunoasterea standardelor RBPF si EHS;
    • Capacitate dе analiză şi sinteză a informaţiilor;
    • Rezistenta la lucrul sub presiune;
    • Disponibilitate dе a invata lucruri noi, abilitati dе comunicare, flexibilitate, simt analitic dezvoltat

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