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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


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


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


  • 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


Driving License
  • Yes