Henkjan Gellekink
Experienced Regulatory Affairs Project Manager with a demonstrated history of working in the pharmaceuticals and medical device industry.... | Nijmegen, Gelderland, Netherlands
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Henkjan Gellekink’s Emails he****@az****.com
Henkjan Gellekink’s Phone Numbers No phone number available.
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Henkjan Gellekink’s Location Nijmegen, Gelderland, Netherlands
Henkjan Gellekink’s Expertise Experienced Regulatory Affairs Project Manager with a demonstrated history of working in the pharmaceuticals and medical device industry. Skilled in U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), Medical Device Directive/Regulation and Regulatory Affairs. Focused professional with a MSc in Medical Biology from Raboud University Nijmegen.
Henkjan Gellekink’s Current Industry Zwiers Regulatory Consultancy
Henkjan
Gellekink’s Prior Industry
Radboud University Nijmegen Medical Centre
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Nv Organon
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Schering Plough Research Institute
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Merck Research Laboratories
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Synthon
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Zwiers Regulatory Consultancy
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Work Experience
Zwiers Regulatory Consultancy
Regulatory Affairs Consultant
Fri Apr 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Synthon
Sr. Regulatory Affairs Project Manager New Products
Thu Sep 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Mar 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
Merck Research Laboratories
Regulatory Affairs Scientist
Sun Nov 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Oct 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)
Schering Plough Research Institute
Regulatory Affairs Scientist
Sat Dec 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Nov 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)
Nv Organon
Regulatory Affairs Scientist
Mon Jan 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Dec 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time)
Radboud University Nijmegen Medical Centre
PhD researcher
Wed May 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Dec 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Henkjan Gellekink Email Addresses
FAQ About Henkjan Gellekink
-
Henkjan Gellekink is located at
Nijmegen, Gelderland, Netherlands -
Henkjan Gellekink is a
Experienced Regulatory Affairs Project Manager with a demonstrated history of working in the pharmaceuticals and medical device industry. Skilled in U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), Medical Device Directive/Regulation and Regulatory Affairs. Focused professional with a MSc in Medical Biology from Raboud University Nijmegen. Zwiers Regulatory Consultancy -
Henkjan Gellekink currently works in the
Zwiers Regulatory Consultancy -
Henkjan Gellekink specializes in
Experienced Regulatory Affairs Project Manager with a demonstrated history of working in the pharmaceuticals and medical device industry. Skilled in U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA), Medical Device Directive/Regulation and Regulatory Affairs. Focused professional with a MSc in Medical Biology from Raboud University Nijmegen. -
Henkjan Gellekink speaks the following languages:
No languages available. -
Henkjan Gellekink has prior experience in the following industries:
Synthon , Merck Research Laboratories , Schering Plough Research Institute , Nv Organon , Radboud University Nijmegen Medical Centre -
Henkjan Gellekink has the following professional experience:
Zwiers Regulatory Consultancy , Synthon , Merck Research Laboratories , Schering Plough Research Institute , Nv Organon , Radboud University Nijmegen Medical Centre . -
You can view Henkjan Gellekink’s
LinkedIn profile at LinkedIn URL. -
Henkjan Gellekink’s work email addresses are
[email protected] . -
Henkjan Gellekink works at
Zwiers Regulatory Consultancy
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