Experience

Medfiles

• Finland
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Regulatory Affairs Manager

  • Mar 2009 - Present

  -Marketing authorization maintenance of human medicinal products -Preparation, submission and management of variation and renewal applications (national and DCP/MRP) -Preparation of Product Information -Pharmacovigilance -Quality Assurance -Project management -Marketing authorization maintenance of human medicinal products -Preparation, submission and management of variation and renewal applications (national and DCP/MRP) -Preparation of Product Information -Pharmacovigilance -Quality Assurance -Project management



Sandoz

• Switzerland
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Regulatory Affairs Officer

  • Jan 2008 - Jan 2009

  -Marketing authorization maintenance of human medicinal products -Preparation of Product Information -Marketing authorization maintenance of human medicinal products -Preparation of Product Information



CTT Cancer Targeting Technologies

• Helsinki, Finland

• Analytical Chemist

  • May 2003 - Dec 2008

  -Responsible for the HPLC environment -Quality Management -Management of IPR data -Responsible for the HPLC environment -Quality Management -Management of IPR data