OPEN POSITION: Analyst in a Quality Control Laboratory
News Open Position

OPEN POSITION: Analyst in a Quality Control Laboratory

Sinceritas is now accepting applications for an ‘Analyst in a Quality Control Laboratory’ position.

Interested? Read more for details on responsibilities and needed qualifications.


  • Efficient and quality execution of all activities within quality control of input substances, packaging, intermediate products and finished products in accordance with GMP requirements
  • Implements GMP and ISO standards requirements
  • Coordinates activities related to the records of each reception of the quality control analyst
  • Monitors the stability of final products and prepares stability studies
  • Actively participates in the development of analytical methods and their validation
  • Participates in in-process product control
  • Organizes the storage of counter-samples from performed analyzes
  • Develops Standard Operating Procedures that regulate and organize activities in the field of quality control
  • Archives documentation in accordance with the established Document Management System
  • Takes care of the proper functioning and maintenance of instruments and laboratory equipment. Performs periodic calibrations, qualifications and prepares reports on performed activities
  • Develops instructions for working with instruments and laboratory equipment. Informs the department manager about all observed defects of the equipment in order to ensure regular servicing, and provide spare parts for it
  • Ensures that the safety standards and cleanliness of the laboratory are observed
  • Train other analysts to conduct laboratory procedures and analyzes
  • Consults professional literature to make suggestions and apply new found knowledge in the field of quality control
  • Reports or investigates suspicious test results. Writes and documents performance reports outside the quality specification
  • Monitors results by parameter and prepares out-of-trend results reports
  • Participates in internal assessments and audits where necessary
  • Prepares reports after completed quality control
  • Takes care of the reference library of standards, actively monitoring their use
  • Participates in the proper implementation of the Quality and Environmental Management System and takes care of a clean and healthy environment
  • Other assigned responsibilities according to skills and qualifications


  • University degree in Pharmacy, Chemistry, Technology, Biology, or related field.
  • A minimum of 2 years of work experience in a QC pharmaceutical laboratory
  • Excellent knowledge of applicable analytical methods and procedures
  • Excellent knowledge of work processes in the pharmaceutical laboratory for quality control, GMP, GLP
  • Experience in performing various laboratory analyzes, working with HPLC, GC-MS, etc.

The Analyst in a Quality Control Laboratory’s working hours are Monday to Friday, 08:30 to 16:30 at the Sinceritas Production Facility in Rosoman, Kavadarci.

If interested in joining #TeamSinceritas, please send your updated resume in English to with the subject line reading: Application for the Analyst in a Quality Control Laboratory’s position

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