Head Of Quality Control – pharmaceutical industry

Employer: ABC Human Capital
Domain:
  • Quality Control
  • Pharmacy - Health
  • Job type: full-time
    Job level: Manager
    Location:
  • BUCHAREST
  • Updated at: 05.02.2023
    Short company description

    ABC Human Capital este urmarea fireasca a experientei castigate de fondatorul companiei, in acest domeniu vast, complex, provocator, in continua miscare si schimbare al resurselor umane.
    Anul 2005 a reprezentat momentul concretizarii unui ideal: fondarea unei agentii de recrutare si executive search ce pune la dispozitia clientilor sai atat consultanta in recrutare si headhunting, precum si intreaga gama de servicii aferente capitalului uman.
    Adaptam cu succes noile tendinte din domeniul Resurselor Umane si utilizam creativ oportunitatile pe care le ofera mediul economic pentru atingerea target-urilor comerciale si de comunicare ale partenerilor nostri.
    Activitatea noastra se traduce in solutii inteligente bazate pe baze de date complete si complexe, aplicatii web, portaluri de informare si socializare, baterii de teste concepute si implementate impreuna cu fiecare dintre parteneri, campanii de marketing online si headhunting.

    Requirements

    Having Bachelor’s Degree in Chemistry and Chemical Engineering.
    Living in Romania
    Being fluent in English.
    Willing to work in night shift.
    Graduated from Chemistry, Chemical Engineering, Pharmacy, and Biology departments of universities.
    3-5 years of work experience in the pharmaceutical industry.

    Responsibilities

    Acts with the responsibility of effective, efficient management, execution, and evaluation of quality control activities.
    Completes all tests related to quality control of chemical and microbiological analysis of primary materials, the packaging materials, intermediary and final products, according to GMP, GLP, GRP, the approved documents, the Radiation and Occupational Health Safety rules and environmental rules reporting, evaluating recording these tests into system.
    Takes part in implementing corrective actions established through internal and international quality audits.
    Ensures the provision of necessary conditions for the use of quality control laboratories in accordance with GMP, GLP, and GRP requirements
    Plans are executed the calibration, validation activities within the Quality Control Laboratory
    Prepares or ensures the preparation of SOP and device information sheets regarding quality control laboratory activities, keeps revelant SOPs up to date, ensures that recording forms in use are up to date.
    Carries out activities regarding the control of environmental conditions
    Takes part in the validation activity of the technological processes, of the analytical methods as well as in the validation activity for the cleaning of the equipment, spaces, and tools, along with the representatives of the departments involved in this activity.
    Takes a continuous process of self-training and takes part in the training related to the carried activity according to GMP.
    Performs and supervises warehouse activities.