Overview
Quality Control Technician Jobs in Riyadh, Saudi Arabia at SRG
Title: Quality Control Technician
Company: SRG
Location: Riyadh, Saudi Arabia
QC Technician
Sudair, Saudi Arabia
Permanent
Sun-Thurs, 8am to 5pm
Salary dependant on skills, background and experience
Role profile:
To work as Team Member of Project Team for Establishment of new Physical and Chemical Analysis division of Quality Control lab (Green Filed Project) for Pharmaceutical Injectable products. To provide support for development, performance and execution of the Quality Control activities for Physical and Chemical Analysis and coordinate respective section Heads/QC Manger on Daily basis.
To support execution of Project related tasks and daily routine operation of Physical and Chemical Analysis division of QC lab and coordinate with Respective Section Head/QC Manager and other departments for timely analysis, investigation and release of Incoming, in-process and finished goods samples and validation samples.
To assist respective Section Head for coordination within Quality Control, Quality Assurance, Production, Engineering, Training and HR department.
To assist respective Section Head for coordination with External Customer i.e. Product Customers, external approved lab, instrument suppliers, calibration agencies etc.
Role requirements:
To perform Sampling and analysis of raw materials, IPC samples, drug substances and drug products and to ensure all documented results are according to cGMP in respect of Chemical/ Analytical.
To support technology transfer of analytical methods to QC, to assist method verification & validation Test sample as per schedule. Perform these tests independently once qualified.
To support the analysis of raw materials, bulk samples, finished products using HPLC, GC, UV Visible, and FTIR Instruments.
To support respective supervisor from QA/QC for handling of incidents & deviations in the laboratory, OOT and OOS.
To support the calibration process of all Lab Instruments and Equipment is as per Standard Operating Procedures. Later perform these tests independently once qualified.
To support cGMP, GLP implementation in daily operations of laboratory activity with emphasis on the documentation.
To support troubleshooting of instruments or other equipment’s if possible.
Complies with all General Laboratory Practices (GLP), safety requirements, laboratory standard operating procedures.
To support in performance qualification, validation studies and routine validation requirements.
Your background:
Bachelor’s degree in pharmacy, Chemistry, Biotechnology, Biochemistry or any other related field.
Master’s degree in pharmacy, Chemistry, Biotechnology, Biochemistry or any other related field.
3 Year in Pharmaceutical/ Biotechnology Manufacturing Organization with EU-GMP environment.
1 years in multi-national Pharmaceutical/ Biotechnology Manufacturing Organization with EU-GMP environment.
Pharmaceutical/ Biotechnology Manufacturing Organization with EU-GMP environment.
Insulin Manufacturing & Contract Manufacturing Organization (CMO)
Validation life cycle for all utilities, Facility, equipment’s, process, cleaning and Media fill.
Risk base approach key tools, Failure Mode Analysis, Risk Assessment Matrix.
