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Summary

over 10 years experience in Pharmaceutical Industry including Clinical research, Regulatory Affairs and Pharmacovigilance. over six years experience in Quality Assurance acting as a quality manager. deputy Qualified Person for Pharmacovigilance (qppv) since 2014. specialities: Auditing, maintenance and tracking of capa, SOP writing, Risk Assessment, gcp Training, computerized system Validation, monitoring

Experiences

Current Experience

  • Deputy QPPV (Qualified Person for Pharmacovigilance)


    Since November 2014

  • Quality manager


    Since August 2007

Past Experience

  • Clinical Research Associate (CRA)

    October 2000 --- July 2007

  • Regulatory Affairs Officer

    April 2004 --- March 2006

  • Regulatory Affairs Officer

    January 1999 --- October 1999

  • Scientist (toxicokinetics)

    December 1997 --- December 1998

Knowledge

LinkedIn Assessment :
GCPClinical monitoringRegulatory affairsPharmacovigilanceClinical trialsCROICH-GCPRegulatory submissionsClinical DevelopmentClinical researchCTMSPharmaceutical IndustryRegulatory RequirementsPharmaceuticsQuality System

Education

  • Vacational teacher in Pharmacy from School of vacational teacher education, Oulu university of applied sciences in 2016
  • MSc (Pharmacy) in Pharmacology from Helsingin yliopisto / University of Helsinki in 1998
  • Ylioppilas (matriculation examination) in from Laanilan lukio in 1991
  • in from Coon Rapids Senior Highschool in 1989

Area / Region

Oulu, Finland

Others

Driving License
  • Yes

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