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Ir. Kristin Heirwegh (°1959)

Educational profile

1983


Bio-engineer
Catholic University of Leuven-Belgium (KULeuven)

1994

IATA certification for shipping of Dangerous goods by Air (Sabena)

2001

Prevention Advisor (‘Preventieadviseur’)

2003 ADR certificate of training as ‘Safety Advisor for the Transport of Dangerous Goods on the road’ in Europe (Certificate N° 0000001388 NL/2495/173/3721 B Ministerie van Wegverkeer; cf KB 1/7/1999)

1996-2002

Supply chain skills: logistics management & logistics auditor; ERP; inventory & warehouse mgmt; shipping of pharmaceutical perishables & dangerous goods; shipping documentation & packaging; cost reduction in purchasing; Environmental, safety & quality aspects for the purchase mgr.

2002-2005

Management skills : Project planning, implementation, control & management review; meeting skills; internal & external communication; marketing & commercial management of projects; safety & environmental auditing; Environmental aspects for the Prevention Advisor; Waste mgmt SME; Risk inventarisation and Prevention planning

2005

Environmental Coordinator ‘Milieucoördinator / Bioveiligheidsadviseur’

 

Professional profile

1983-1984

Assistant-interimaris Lab Tropical Plant Research of KULeuven- Genecollection

1984-1986

Scientific collaborator Virology lab at the Rega institute KULeuven (Prof. A.Billiau; Multiple Sclerosis)

1986-1994

1986-1994 Scientific collaborator at Innogenetics nv Gent and at the Immunology Lab of the Free University of Brussels (VUB; Prof. De Baetselier)

1994-1999

Logistic manager of R&D at Innogenetics nv Gent

1999

Purchase manager of Production and R&D at Innogenetics nv Gent

1999-03/2002

Materials manager (production planning & inventory) of Production and R&D at Innogenetics nv Gent

16/03/2002

Scientific collaborator of BioMaric nv Gent

01/01/2003

Operations manager of AIP nv Gent


Research experience
Cell culturing; development of monoclonal antibodies; development of qualitative & quantitative screening tests for immunological & biological activity of antibodies & cytokines; protein purification.

Consulting experience
Assisting companies with the implementation of a dynamic risk management system to be compliant with European Safety & Welfare Legislation (paper free tool for follow-up); assisting with the implementation of transport regulations for life science goods as organs, GMO’s, blood samples, diagnostic tests, dangerous goods, …; developing & implementing follow-up systems for (internet based) purchasing, stockvaluation & -management.

 
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