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Karin Baas is listed as Independent Consultant / QA Specialist based in Greater Groningen Area, Netherlands, Netherlands. AeroLeads shows a work email signal at mac.com and a matched LinkedIn profile for Karin Baas.
Karin Baas previously worked as Independent Consultant at Quality & Risk Management Zw-Frl and QA Specialist (Consultant) at Qps Netherlands B.V.. Karin Baas holds M.Sc., Clinical Research from Cardiff University / Prifysgol Caerdydd.
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QUALITY & RISK MANAGEMENT zw-frl is offering independent GxP consultancy. The consultancy is offered by Karin Baas, GxP and QA expert with more than 25 years of experience within Pharmaceutical Industry, Medical Device Industry and CRO Business.. Karin Baas is an active member of DARQA (member of the GCP committee).
Listed skills include Gmp, Quality System, Medical Devices, Iso 13485, and 15 others.
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The Netherlands
In Summer 2014 I have started up my own GxP consultancy company.I work as an independent consultant, mainly in the area of GCP, GLP, GcLP and GMP. My backpack is loaded with more than 20 years of experience in Pharmaceutical Industry, Medical Device Industry and CRO Business.Should you need GxP/Compliance/Quality Systems/Risk Management advise.
Responsible for Quality Management within the organization.
Xendo Drug Development has been aquired by QPS.
Several QA Management positions, for R&D and GMP business processes.
Responsible for internal auditing (clinicial study files, processes, etc) and clinical study auditing (clinical sites).
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Karin Baas is listed as Independent Consultant / QA Specialist.
AeroLeads has found 1 work email signal at @mac.com for Karin Baas.
Karin Baas is based in Greater Groningen Area, Netherlands, Netherlands.
Karin Baas has worked for Quality & Risk Management Zw-Frl, Qps Netherlands B.V., Qps Netherlands Bv (Qps Aquired Xendo Per 23 July 2010), Xendo Drug Development, and Cordis Europa Nv.
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Karin Baas holds M.Sc., Clinical Research from Cardiff University / Prifysgol Caerdydd.
Karin Baas is listed with skills including Gmp, Quality System, Medical Devices, Iso 13485, Glp, Quality Assurance, Pharmaceutical Industry, and Capa.
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