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Jan Slováček

Deputy Head Of Validation Team at QUINTA-ANALYTICA

Jan Slováček is a Pharmaceutical Validation Analyst at QUINTA-ANALYTICA, a position held since April 2016, with expertise in HPLC, IC, and ICP-MS methods. Previously, Jan worked as an HPLC and ICP-MS Analyst focusing on the development of ICP-MS methods. Prior experience includes a role in administrative and operational tasks at Pilulka Distribuce s.r.o. Jan Slováček holds a Master's degree in Analytical Chemistry from Charles University (2014-2016) and a Bachelor's degree in Clinical and Toxicological Analysis from the same institution (2011-2014). Jan completed secondary education at Dvořákovo gymnázium a SOŠE Kralupy nad Vltavou, earning a maturita in 2011.

Location

Prague, Czech Republic

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QUINTA-ANALYTICA

Quinta is a GCP/GLP/GMP-certified, EMA and FDA-inspected European CRO offering in-house clinical testing, pharmaceutical analysis, CMC and R&D. Quinta specializes in clinical studies, bioanalytics, method development and quality control for both small and large molecules, human and veterinary IMPs as well as generics. We provide unrivaled expertise to worldwide pharmaceutical and biotechnological clients across the entire pharma spectrum. Quinta is part of the Conscio group with headquarters in Munich, Germany, laboratories in Czechia, Austria, Slovakia, Germany and offices in the USA. Our main service areas include: 1) Clinical Testing: With 2 in-house clinical units providing BE/BA/PK studies, with capacity for 60+40 beds. 2) Bioanalytical Testing: GLP/GCP solutions for preclinical & clinical studies, small & large molecules, BE/BA/PK. 3) Research & Development: Analytical R&D, impurities, extractables & leachables, degradation, trace studies. 4) Pharmaceutical Quality Control: GMP quality control, batch testing, stabilities, HAPIs, inhalation, API sourcing. 5) Microbiology: GMP sterile & non-sterile testing, microbial/water analyses, endotoxins, antibiotics & vitamins. 6) Biopharmaceutical Quality Control: GLP/GMP bioanalysis, CMC, characterizations of peptide & protein IMPs, biosimilars. Quinta was founded in 1997 and has been successfully inspected by FDA more than 10 times. Quinta is headquartered in Prague, Czech Republic.


Employees

51-200

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