Parcourir les catégories
Explorer
Fiverr Pro
Français
$
USD
Oduzgun
@ozgedzgn
Turquie
Turc, Anglais
À propos de moi
-I developed a new analytical method for the quantification of coumarin in goldenseal by HPLC according to -
ICH and wrote my thesis by performing analytical method validation of this method. I have worked in quality
control, quality assurance and R&D in the pharmaceutical, cosmetics, food supplements, paint, plastics and
biocidal products industries.
-I have managed studies and validation processes according to international standard methods such as the
European pharmacopoeia, ICH, WHO and FDA, and reported on the processes. I am experienced in research
and development, reporting, method
Compétences
Oduzgun
hors ligne •
Voir mes services
Business
I will develop and validate analytical methods according to ich
Gestion de projet
I will write sops for gmp, glp, iso 17025, quality systems
Expérience professionnelle
Quality Control Officer
PharmEasy • Temps plein
Jul 2020 - Aug 2024 • 4 yrs 1 mo
To control the work according to GMP, GLP and hygiene rules and to make arrangements, updates, etc. when necessary -To perform, report and control the semi-finished and full-product analyzes of the products (to determine the amount of the desired component in the product with devices such as HPLC, GC, Spectrophotometer) -To take water, raw material, packaging samples, to perform physical and chemical analyzes, to report -Preparation of solutions required for product, raw material and packaging analysis -To carry out the acceptance/rejection procedures and label procedures of products, raw materials and packaging materials, -To prepare Analytics, Transfer Analytics, Process and Cleaning validation protocols/reports, to analyze, report and control -To carry out product and raw material analysis method development studies, to create analysis methods -To follow up approved raw material and packaging material manufacturers and suppliers, -To prepare, revise and control the Quality Control Department Standard Operating Procedures -To carry out annual evaluation studies of raw materials, products and packaging materials -To keep records showing that all necessary sampling and analysis procedures have been carried out, to record and investigate any deviations -Preparing CTD file for licensing procedures -To carry out stability analyses, report and control
