QC Specialist at Global Napi Pharmaceuticals
Location: 6th of October, Giza
Job Description
Ability to understand and comply with GMP & GLP
Operate with proficiency of lab instruments.
Issues the test reports /Certificate of analysis for reviewing by lab. Head.
Preserve and store samples as per the approved methods.
Inspect received samples and ensure all in compliance with standard requirements
Follow up all equipment cleaning, record in related forms
Ensure all records and files are kept in the designated locations.
Issue work records, log books, chromatograms and calculated results
Performs analysis of drug concentrations using HPLC, Atomic absorption, GC, UV spectroscopy or IR.
Perform the intermediate checks of the lab equipment’s to ensure the accuracy and validity of the equipment
Recording and follow up of the temperature, housekeeping in the lab. Calibration of equipment.
Secures the compliance with quality standards (ISO 9001:2015), environment (ISO14001) and safety (ISO 45001) requirements according to national and international standards.
Assuring of results by means of control charts and PT Scheme.
Job Requirements
B.Sc. in Chemistry or Pharmaceutical Sciences, preferably Pharmaceutical Sc.
Years of professional experience vary according to the Career Ladder Scheme
Work experience in a GMP/GLP regulated environment.
Ability to understand and comply with GMP & GLP.
Good common sense and judgment skills.
Able to identify, analyze and solve problems.
Good chemistry knowledge and analytical chemistry lab experience.