Laboratory Equipment Validation Consultant At PQE Group
Job description
PQE Group is a Contract Quality Organization and a Complete Quality Solution provider for GCP, GLP, GMP & GDP areas in the Life Science Industry. Since 1998, we have successfully completed more than 7,000 projects worldwide and now serve our Clients from offices in Italy, Spain, Switzerland, Germany, LATAM, USA, the Middle East, China, India and Japan. As an international group we have experience working in more than 25 languages and have an excellent history of supporting small, medium and large size companies exceeding compliance standards from the FDA / EMA / WHO / TGA / SFDA / ANVISA / INVIMA / GILS and other local authorities.
Due to a constant growth, PQE is looking for a new Lab Equipment Validation Consultant in Alexandria, Egypt.
Responsibilities:
Perform equipment lifecycle activities and associated deliverables pertaining to laboratory instruments and equipment, including but not limited to the installation, testing, execution of validation activities, calibration, maintenance, change control, retirement activities, the renewal of laboratory instrumentation and equipment service contracts as well as assisting on-site vendor maintenance procedures per contract agreement.
Schedule maintenance and calibration of lab equipment.
Maintain the records of calibration. Assist in maintain and monitor equipment and instrumentation data in the computerized maintenance management system up to date.
Maintain equipment inventory and ensure that preventative maintenance is performed according to the manufacturer’s requirements and Standard Operating Procedures.
Ensuring preventive maintenance is performed according to manufacturer’s requirements and internal Standard Operating Procedures (SOPs).
Requirements:
Degree in a scientific discipline (with strong chemistry content).
1 years of experience working in a QC lab setting
Highly proficient in the use of key analytical equipment (HPLC, GC, IR, UV) and the testing of finished products.
Experience of working in a GMP environment.
Good IT skills e.g. Microsoft Office (Word, Excel and Outlook).