Qualimetrix S.A. is a third-party Contract Research Organization, established in 2013, that provides analytical services to pharmaceutical industry.
Qualimetrix S.A. is involved in the development of the Quality part of pharmaceutical products (module 3) as well as in RnD, QC activities and QP services.
In the frame of its activities Qualimetrix S.A. is recruiting a Manager for the Quality Control Department based in company's laboratory in Athens, Greece.
Chief Science Officer
Approves specifications, test methods and Quality Control procedures.
Holds responsibility for the proper implementation of the quality controls procedures by the department’s personnel.
Reviews quality control procedures, protocols and EOI’s.
Overviews the QC department analytical activities.
Holds responsibility for the timely and proper training of the quality control personnel, provides all relevant SOP’s and instructions, verifies the ability to undertake the responsibilities delegated to them in a study and adapts training according to need.
Holds responsibility for the management of laboratory equipment and for the management of all record keeping relating to the above, and to ensure the qualification and maintenance of his department, premises and equipment.
Ensures the appropriate validations are performed.
Manages all quality control activities.
Holds responsibility for the maintenance of the department’s physical archive
Manages the OOS procedure
Provides technical assistance regarding the results / procedures / analytical equipment, internally and externally as required
Ensures that all necessary testing is carried out and the associated records evaluated
Participates in management reviews and advocates continual improvement
Contributes to suppliers and sub-contractor’s evaluation
Work experience requirements
5 years’ experience with analytical techniques
2 years’ experience in a GMP oriented laboratory
Minimum requirements :
BSc in Chemistry or Pharmacy
MSc in Chemistry / Pharmaceutical Analysis
Training on principles of GMP
Excellent knowledge of the English language (CEFR Level B2)
Excellent knowledge of Microsoft Office applications
Preferred requirements :
PhD in Chemistry / Pharmaceutical Analysis
Friendly corporate culture
High level training on GMP and related fields
Scientific working environment with strong motivating character