по договоренности
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European pharmaceutical company.

Job Responsibilities:

  • Writing/updating SOPs and operational instruction;
  • Track the SOPs list/QMS Plan – control of timely implementation and updating;
  • Carrying out/control/documentation actions for CAPA, Deviations, Change control (etc.) processes
  • Documentation management;
  • Responsible for trainings of newcomers; annual trainings for all staff;
  • Support audits/quality checks activities if required (administrative/organizational);
  • Routine daily checks of HA database (check the presence of official prescriptions);
  • Documentation (registration in the file, printing, archiving).
  • Conclusion of contracts with laboratories/service suppliers (for purchasing chemical reagents, reference standards);
  • Organization of independent expertizes in laboratories upon VALEANT initiative
  • Organizational and administrative support of GMP-inspections;
  • Support for quality queries;
  • Ordering reference standards upon request;
  • Cross functional collaboration in projects with QA involvement
    • Work Environment:

    • Office - close to Shabolovskaya metro station.
    • Competitive salary level.
    • Corporate medical and life insurance, annual bonus, mobile phone compensation.
      • Requirements:

      • Work experience: 3 years in pharmaceutical company
      • English language: intermediate
      • Education: higher education (chemistry, biology, pharmacy specialization)
      • Additional: stress-resistance, multitasking skills, PC advanced user, knowledge of local and international standards, the possibility for business trips (warehouses in Moscow district)
      • Knowledge of local legislation, international standards and practices for medicinal products and medicinal devices is a plus.
        • Тип занятости:

          Полная занятость, полный рабочий день, у работодателя

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