Farmaprojects looks for a QC Specialist to be part of our laboratory for a long term position.  This position will report directly to the QC Manager and the main responsibilities will be:

  • To carry out the necessary analysis and control functions in order to effectively cover the existing needs in the Quality Control department.
  • To perform the appropriate tasks to streamline and make the necessary processes profitable.
  • Ensure compliance with the Rules of GMP (Good Manufacturing Practices)
  • Ensure compliance with GLP.
  • Conducting the sampling and analysis according to approved procedures (applying GLP) of API, and finished product.
  • Completion of the analysis bulletins with the agreed results and immediately inform the immediate supervisor of any non-compliance found for its assessment and control.
  • Collaboration in forecasts of material, tools, etc.
  • Responsibility for operation and calibration of the assigned devices and installations.
  • Compliance with all the SOP (Standard Operation Procedures) existing in the Company related to their work.
  • Keep the file updated of all the generated documentation.
  • Support the QC Manager when required. Provide ideas regarding aspects of improvement, solutions and new working procedures.
  • Perform technical reviews and calculations generated in the laboratory.
  • Keep the laboratory tidy and clean. Ensure the correct handling, maintenance and calibration and cleaning of laboratory equipment.
  • Collaborate in the drafting and updating of SOP standardized work procedures
  • Collaborate in the investigation of analytical deviations and out-of-specification     results.
  • Compliance with quality, safety, prevention and environmental standards.
  • Maintain the general organization of the laboratory (standards, components, laboratory material, samples, etc.) and promote an adequate work environment.

Minimum requirements:

  • Laboratory Technician. Chemistry or Pharmacy Degree.
  • Minimum 3-5 years’ experience in the pharmaceutical industry analysing FDF
  • High experience using EMPOWER (HPLC WATERS).
  • High experience working under GMP regulations.
  • High level of English is essential, at a contract drafting and negotiation level.