Qualimetrix S.A. is a third party Contract Research Organization, established in 2013, that provides analytical services to the 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 an Assistant Officer for the laboratory, based in the company's premises in Athens, Greece.
Reports to the Department’s Supervisor
Responsibilities
- Holds responsibility for the tidiness and cleanliness of the laboratory area including auxiliaries/ glassware sterilization and waste destruction
- Prepares solutions for the daily operations and housekeeping (e.g. cleaning solutions)
- Notifies, in a timely manner, the department’s supervisor in case of instrument failure or any other malfunction.
- Informs the department’s supervisor in case of lack of resources for the proper operation of the laboratory
- Contributes to the laboratory’s stock monitoring regarding analytical reagentsand consumables
- Performs culture media preparation and growth promotion testing
- Performs routine environmental monitoring of controlled areas, including air sampling, surface sampling, and purified water analysis
- Assists with the maintenance and/or periodic calibration/qualification of the laboratory’s equipment
- Provides assistance to the department’s officers in lab operations and testing
Work experience requirements
- One year experience in a microbiological laboratory (preferably under GMP)
Education requirements
Minimum requirements:
- Technological Education Institute / Post-secondary degree (T.E.I. or I.E.K.) in Biology, Chemistry, Food technology or relevant fields.
- Good knowledge of the English language (CEFR Level B2)
- Basic knowledge of Microsoft Office applications
Preferred requirements:
- Training in GMP principles
Company offers
- Competitive salary
- Friendly corporate culture
- Private insurance
- High level training on GMP, technical and regulatory aspects of current industry trends and requirements