10.2020 - present, Embryologist | Seminologist, Embryology and Andrology Laboratory, Cryobank, Parens Warszawa - Fertility Clinic
→ ANDROLOGY: CASA-assisted semen analysis, concentration, motility, vitality, morphology; Mixed antiglobulin reaction (MAR) test; Hyaluronan binding assay (HBA) to asses sperm maturity; Sperm vitrification; Sperm preparation - simple washing, direct swim-up, density gradient, ZyMot; Preparation for intrauterine insamination; matching donor semen for patients, intra uterine insemination with donor sperm (AID)
→ EMBRYOLOGY: Performing IVF procedures: Eggs retrieval, denudation, ICSI, pICSI, embryos grading, transfers, oocyte and embryo vitrification, thawing of oocytes and embryos, artificial oocyte activation, laser assisted hatching (AH);
09.2020 - 10.2020, Laboratory scientist | Seminologist, Andrology and Seminology Laboratory, OVIklinika | ProVIta Sp. z o.o. - Fertility Clinic
→ Determination of hormone blood levels using immunochemical analyzer by Roche - Cobas e411. Carrying out regular maintenance of the analyser, performing calibration and precision control;
→ Carrying out CASA (Computer Assisted Semen Analysis) analysis, assessment of concentration, motility and morphology of the semen samples;
→ Assessment and preparation of semen for in-vitro fertilization, intrauterine insemination;
→ Assessment of vaginal biocenosis from vaginal smear slides;
→ Completing necessary paperwork regarding reproductive cells preparations, in-vitro fertilization, according to local Government requirements.
01.2017 - 03.2018, Safety Data Specialist (Pharmacovigilance), Merck Sharp & Dohme Poland, Warsaw, Poland
Analysing, triaging, and processing all adverse experience information received for all products according to standard operating procedures for reporting to worldwide regulatory agencies.
→ Perform data entry/review of all adverse experience information received and processed within safety database within the established timeframes to ensure compliance with internal, business partner, and regulatory agency reporting requirements worldwide.
→ Participate/perform in training and certification activities for GPVO.
→ Collaboration with staff within the organisation as well as cross-functionally.