Τοποθεσία Αγία Παρασκευή πριν 4 μέρες Ημ. ανάρτησης πριν 4 μέρες Με κάποια εμπειρία Επίπεδο εμπειρίας Με κάποια εμπειρία Πλήρης απασχόληση Τύπος απασχόλησης Πλήρης απασχόληση Επιστημονικός Κλάδος Κατηγορία θέσης Επιστημονικός Κλάδος
QC Supervisor

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 Analytical Development, QC activities, QP services and GLP studies.

In the frame of its activities Qualimetrix S.A. is recruiting a QC Supervisor for the Quality Control Department based in company's premises in Athens, Greece.

Reports to

QC Manager

Responsibilities

Performs the review of requests for the new studies undertaken by the QC Department.

Holds responsibility for the preparation of a new study undertaken before its execution by the involved laboratory department.

Contributes to the planning of the studies executed by the QC Department (overall and daily planning) and communicates it to the analysts.

Prepares and reviews quality control procedures, protocols and EOI’s.

Overviews and coordinates the QC department analytical activities.

Provides technical assistance for the analytical activities of the department.

Holds responsibility for the monitoring and implementation of the equipment maintenance and qualification schedule for the department

Identifies and reports to the QC Manager the needs of the department regarding additional/new equipment and contributes in its selection (URS compilation etc.) and purchase.

Authors the final reports for the analytical studies (e.g. Certificate of Analysis, Stability Card etc.)

Identifies, documents and reports analytical issues, OOS and deviations that may affect results and participates in the department’s events investigations

Holds responsibility for the department’s physical archive.

Contributes in the development and validation of the analytical calculations excel worksheets.

Contributes in the training of QC officers.

Provides assistance to the QC Manager.

Work experience requirements

Two (2) or more years’ experience with analytical method validation under GMP environment.

Education requirements

Minimum requirements:
BSc in Chemistry or Pharmacy

Excellent knowledge of the English language (CEFR Level C2)

Excellent knowledge of Microsoft Office applications

Preferred requirements:
MSc in Chemistry/Pharmaceutical Analysis

Training on principles of GMP

Company offers

• Competitive salary
• Private insurance
• Friendly corporate culture
• High level training on GMP and related fields
• Scientific working environment with strong motivating character