Mateja Gspan Msc
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Mateja Gspan Msc Email & Phone Number

Regional Head of Pharmacovigilance and Business Compliance at Lenis farmacevtika d.o.o.
Location: Slovenia, Slovenia, Slovenia 8 work roles 3 schools
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Current company
Role
Regional Head of Pharmacovigilance and Business Compliance
Location
Slovenia, Slovenia, Slovenia
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Who is Mateja Gspan Msc? Overview

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Mateja Gspan Msc is listed as Regional Head of Pharmacovigilance and Business Compliance at Lenis farmacevtika d.o.o., a company with 30 employees, based in Slovenia, Slovenia, Slovenia. AeroLeads shows a matched LinkedIn profile for Mateja Gspan Msc.

Mateja Gspan Msc previously worked as Regional Head of Pharmacovigilance & Business Compliance at Lenis Farmacevtika D.O.O. and Regional Pharmacovigilance & Business Compliance Manager at Medicopharmacia at Medicopharmacia D.O.O.. Mateja Gspan Msc holds Bachelor Of Biological Science (B.Sc.), Plant Tissue Cultures, Secondary Substances from University Of Ljubljana, Biotechnical Faculty, Department Of Biology.

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Lenis farmacevtika d.o.o.

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About Mateja Gspan Msc

Mateja Gspan Msc is a Regional Head of Pharmacovigilance and Business Compliance at Lenis farmacevtika d.o.o.. They possess expertise in regulatory submissions, regulatory affairs, quality management, gmp, pharmacovigilance and 13 more skills. They is proficient in English, German and Croatian.

Listed skills include Regulatory Submissions, Regulatory Affairs, Quality Management, Gmp, and 14 others.

Current workplace

Mateja Gspan Msc's current company

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Lenis farmacevtika d.o.o.
Lenis Farmacevtika D.O.O.
Regional Head of Pharmacovigilance and Business Compliance
Slovenia
Website
Employees
30
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8 roles · 9 years

Mateja Gspan Msc work experience

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Regional Head Of Pharmacovigilance & Business Compliance

Current

Ljubljana, Slovenia

Jan 2022 - Present

Regional Pharmacovigilance & Business Compliance Manager At Medicopharmacia

Medicopharmacia D.O.O.

Ljubljana, Slovenia

2017 - Jan 2022

Ra/Pv/Qa Specialist

Mateja Gspan S.P.

- full range of services related to Regulatory Affairs (RA) of medicinal products, medical devices, food supplements, cosmetics, biocides- preparation/revision of SOPs for RA and pharmacovigilance (PV) activities- preparation of Clinical Evaluation Reports for medical devices - clinical trials: initial submissions/substantial amendments and other.

Oct 2015 - Jun 2018

General Manager And Regulatory Specialist

Icaro D.O.O. (International Clinical And Regulatory Organization)

Bravničarjeva 13, Ljubljana, Slovenia

- preparation and implementation of Quality Management System/SOPs for new RA&PV Department- tasks and responsibilities of Quality Person for Pharmacovigilance (QPPV)

Oct 2013 - Sep 2015

Regulatory Specialist

Adax International D.O.O.

Bravničarjeva 13, Ljubljana, Slovenia

- preparation and implementation of RA/PV SOPs for medicinal products and medical devices - coordination and performance of RA procedures (e.g. variations, transfers)

Jan 2013 - Sep 2013

Regulatory Affairs Manager

Lek Pharmaceuticals D.D. – Member Of Sandoz Group, Ljubljana, Slovenia

Verovškova 57, Ljubljana, Slovenia

- planning and implementation of registration strategies for new medicinal products in RCC for SEE/CIS region- ensuring up to date product information & managing packaging components (mock-ups, artworks)- cooperation with Lek´s departments and Sandoz´s RCCs - preparation and maintenance of consolidated registration files in MRC

Jan 2001 - Dec 2008

Research Assistant

Institut Für Medizinische Chemie Und Biochemie, Innsbruck, Austria

Fritz-Pregl-Str. 3, Innsbruck, Austria

Main activities and responsibilities: mammalian cell cultures breeding, testing of antiproliferative substances in the cell cultures, radiolabeling of inositol and phospholipids, analysis of cell components by HPLC, detection of intracellular proteins in particular Harvey Ras oncogene by Western Blot analysis.

Apr 1992 - Aug 1993
Team & coworkers

Colleagues at Lenis farmacevtika d.o.o.

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3 education records

Mateja Gspan Msc education

Bachelor Of Biological Science (B.Sc.), Plant Tissue Cultures, Secondary Substances

University Of Ljubljana, Biotechnical Faculty, Department Of Biology

Master Of Science (M.Sc.), Plant Tissue Cultures, Secondary Substances, Information System Design

The National Institute Of Biol., Faculty Of Natural Sciences And Engineering, Ljubljana, Slovenia

Teacher Of Biology

University Of Ljubljana, Biotechnical Faculty, Department Of Biology
FAQ

Frequently asked questions about Mateja Gspan Msc

Quick answers generated from the profile data available on this page.

What company does Mateja Gspan Msc work for?

Mateja Gspan Msc works for Lenis farmacevtika d.o.o..

What is Mateja Gspan Msc's role at Lenis farmacevtika d.o.o.?

Mateja Gspan Msc is listed as Regional Head of Pharmacovigilance and Business Compliance at Lenis farmacevtika d.o.o..

Where is Mateja Gspan Msc based?

Mateja Gspan Msc is based in Slovenia, Slovenia, Slovenia while working with Lenis farmacevtika d.o.o..

What companies has Mateja Gspan Msc worked for?

Mateja Gspan Msc has worked for Lenis Farmacevtika D.O.O., Medicopharmacia D.O.O., Mateja Gspan S.P., Icaro D.O.O. (International Clinical And Regulatory Organization), and Adax International D.O.O..

Who are Mateja Gspan Msc's colleagues at Lenis farmacevtika d.o.o.?

Mateja Gspan Msc's colleagues at Lenis farmacevtika d.o.o. include Marko Koder, Vesna Bizjak, Robert Jesenko, Špela Drnovšek, and Tinkara Žula.

How can I contact Mateja Gspan Msc?

You can use AeroLeads to view verified contact signals for Mateja Gspan Msc at Lenis farmacevtika d.o.o., including work email, phone, and LinkedIn data when available.

What schools did Mateja Gspan Msc attend?

Mateja Gspan Msc holds Bachelor Of Biological Science (B.Sc.), Plant Tissue Cultures, Secondary Substances from University Of Ljubljana, Biotechnical Faculty, Department Of Biology.

What skills is Mateja Gspan Msc known for?

Mateja Gspan Msc is listed with skills including Regulatory Submissions, Regulatory Affairs, Quality Management, Gmp, Pharmacovigilance, Clinical Trials, Fda, and Change Control.

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