Adrianna Kapuscinska
Junior Expert in Safety Data Sheets at THETA Consulting Sp. z o.o.- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
Topline Score
Bio
Credentials
-
Regulatory Affair Specialist
Kariera w FarmacjiJan, 2021- Nov, 2024 -
Safety Data Sheet in accordance with the 2020/878/UE regulation
THETA Doradztwo TechniczneDec, 2020- Nov, 2024 -
HPLC troubleshooting and European Pharmacopoeia methods optimalization
PhenomenexJan, 2016- Nov, 2024 -
Increasing LC productivity and achieving optimal HPLC/UPLC performance
PhenomenexJan, 2016- Nov, 2024 -
Laboratory Workshop HPLC
Bioszkolenia.plJan, 2015- Nov, 2024
Experience
-
THETA Consulting Sp. z o.o.
-
Poland
-
Chemical Manufacturing
-
1 - 100 Employee
-
Junior Expert in Safety Data Sheets
-
Jun 2021 - Present
-
-
-
Middle Tennessee State University (MTSU)
-
United States
-
Higher Education
-
700 & Above Employee
-
Quality Analyst
-
Jan 2020 - Dec 2020
- Developing and writing standard operating procedures including instructions for the instruments as well as general laboratory procedures. - Developing methods and verification of standard methods for fermented beverages, especially wines and juices. - Preparing tests and instructions for Fermentation Science students and co-conducting lab classes. - Developing and writing standard operating procedures including instructions for the instruments as well as general laboratory procedures. - Developing methods and verification of standard methods for fermented beverages, especially wines and juices. - Preparing tests and instructions for Fermentation Science students and co-conducting lab classes.
-
-
-
SENSILAB
-
Slovenia
-
Pharmaceutical Manufacturing
-
100 - 200 Employee
-
Quality Control Analyst
-
Apr 2019 - Dec 2019
- Working in Quality Control Department with GMP requirements - Testing products from various production stages utilizing different analytical techniques, such as HPLC, spectrophotometer, titration - Leading on stability tests of pharmaceutical products - Preparing reports and documents in accordance with requirements - Monitoring data integrity - Participation in OOS activities - Cooperating with QA, R&D and client’s laboratory. - Working in Quality Control Department with GMP requirements - Testing products from various production stages utilizing different analytical techniques, such as HPLC, spectrophotometer, titration - Leading on stability tests of pharmaceutical products - Preparing reports and documents in accordance with requirements - Monitoring data integrity - Participation in OOS activities - Cooperating with QA, R&D and client’s laboratory.
-
-
-
DOZ S.A.
-
Poland
-
Pharmaceutical Manufacturing
-
400 - 500 Employee
-
Product Presentation Specialist
-
Aug 2018 - Mar 2019
- Work in E-Commerce - Participating in creating DOZ.pl website content - Creating unique product descriptions - Work in E-Commerce - Participating in creating DOZ.pl website content - Creating unique product descriptions
-
-
-
Aflofarm Farmacja Polska Sp. z o.o
-
Poland
-
Pharmaceutical Manufacturing
-
300 - 400 Employee
-
R&D Analyst
-
Aug 2015 - Jul 2018
- Working in R&D Department - Developing analytical methods for new medicinal products, dietary supplements, foodstuffs and cosmetics - Leading on stability tests - Operating measuring instruments, such as HPLC, GC, spectrophotometer, dissolution tester, Karl Fisher titration - Working with Ph. Eur. monographs, USP monographs and scientific articles - Preparing reports and documents in accordance with law requirements - Participation in process of transferring analytical method and cooperating with QC. Show less
-
-
Education
-
University of Lodz
Master’s degree, Analytical Chemistry -
Pharmaceutical High School in Lodz
Pharmaceutical technician -
University of Lodz
Bachelor’s degree, Chemistry