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Gerhard   Hartmann


Mainz
XING Profil

Berufserfahrung

2020-07 - heute
QA & CSV Spezialist
Pharmazeutischer Hersteller

2002-08 - 2021-05
Senior Validation Consultant
Biotech - Startup

2000-11 - 2017-07
Senior Validation Consultant
Internationaler Hersteller von Medizinprodukten

2015-12 - 2016-12
Senior Validation Consultant, QA Manager
Medical Device Manufacturer

2016-04 - 2016-07
GMP Senior Auditor
Blood Product Manufakturer

2015-12 - 2016-01
Senior Validation Consultant
Laboratory Services Provider

2015-08 - 1991-07
Senior Validation Consultant
International Pharmaceutical Manufacturer (Germany)

2014-12 - 2015-06
Senior Validation Consultant, QA Manager
Supplier for pharmaceutical industry (IT Solutions)

2015-02 - 2015-05
Senior Validation Consultant
Supplier for pharmaceutical industry (IT Solutions)

2015-02 - 2015-04
Senior Validation Consultant
Supplier for pharmaceutical industry (IT & Hardware Solutions)

2014-07 - 2014-12
Senior Quality Management Consultant
International Manufacturer of Analytical Systems (USA, German locations)

2014-05 - 2014-07
Senior Validation Consultant
International Medical Device Manufacturer (Germany)

2014-01 - 2014-07
Senior Validation Consultant
International Pharmaceutical Manufacturer (Germany)

2004-11 - 2013-12
Senior Validation Consultant, QA Manager
International Pharmaceutical Manufacturer (German)

2009-01 - 2012-01
Validation Consultant, Auditor
International Pharmaceutical Manufacturer (Japan), German facilities

2010-11 - 2011-12
Validation Consultant, Auditor
International Medical Device Company, (US)

2011-11 - 2011-11
QM Auditor
International Pharmaceutical Manufacturer (German)

2010-12 - 2011-03
QM Auditor
International Medical Device Company, (Switzerland)

2011-01 - 2011-01
QM Auditor
International Medical Device Company, (Germany)

2007-04 - 2007-11
Validation Consultant
National Medical Device Manufacturer (Germany)

Berufsausbildung

Chemie

Sprachkenntnisse

Deutsch Muttersprache, Englisch Fließend

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