Lene von Voss

In vivo Laboratory Technician at Gubra
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Contact Information
us****@****om
(386) 825-5501
Location
Copenhagen, Capital Region, Denmark, DK
Languages
  • English Professional working proficiency

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Experience

    • Denmark
    • Biotechnology Research
    • 100 - 200 Employee
    • In vivo Laboratory Technician
      • Oct 2017 - Present

    • Denmark
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Laboratory Technician
      • Aug 2010 - May 2017

      My responsibilities include • Protocol and amendment writing. • Handle the planning, execute and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Catheterisation of pigs. • Collected data for pharmacokinetic and pharmacodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk quality. • Recording in… Show more My responsibilities include • Protocol and amendment writing. • Handle the planning, execute and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Catheterisation of pigs. • Collected data for pharmacokinetic and pharmacodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk quality. • Recording in Electronic laboratory notebook. • Refine dosing and animal models. • Animal welfare/etics - Follow Novo Nordisk standards for working with laboratory animals. • Writing and maintain Procedure. • Presentation of data. Show less My responsibilities include • Protocol and amendment writing. • Handle the planning, execute and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Catheterisation of pigs. • Collected data for pharmacokinetic and pharmacodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk quality. • Recording in… Show more My responsibilities include • Protocol and amendment writing. • Handle the planning, execute and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Catheterisation of pigs. • Collected data for pharmacokinetic and pharmacodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk quality. • Recording in Electronic laboratory notebook. • Refine dosing and animal models. • Animal welfare/etics - Follow Novo Nordisk standards for working with laboratory animals. • Writing and maintain Procedure. • Presentation of data. Show less

    • United States
    • Chemical Manufacturing
    • 700 & Above Employee
    • Regulatory Affairs Associate
      • Apr 2007 - Jul 2010

      My responsibilities included • Preparing and update Safety Data Sheets (according to the defined standard of quality). • Labelling control and update. • Responsible for Personal Care products in Denmark meet the Danish regulation. • Support and communication intern to Marketing, product managers, salesmen, our Dutch laboratory and factories. • Reporting products to the Danish “produktregisteret”. • Prepare Certificate of analysis (CoA). • Customer… Show more My responsibilities included • Preparing and update Safety Data Sheets (according to the defined standard of quality). • Labelling control and update. • Responsible for Personal Care products in Denmark meet the Danish regulation. • Support and communication intern to Marketing, product managers, salesmen, our Dutch laboratory and factories. • Reporting products to the Danish “produktregisteret”. • Prepare Certificate of analysis (CoA). • Customer Service. • Responsible for the Laboratory. • Ensure weekly documentation of Carlsbergs washing plant for bottles were following the defined standard of quality. • Prepare Certificate of analysis (CoA). • Receiving incoming reclamations of chemical products, register and analyse for inorganic parameters. • Inorganic analysis off products among others as pH, spectrophotometric determination of minerals, acid/basic determination. • Reporting results to the product managers. Show less My responsibilities included • Preparing and update Safety Data Sheets (according to the defined standard of quality). • Labelling control and update. • Responsible for Personal Care products in Denmark meet the Danish regulation. • Support and communication intern to Marketing, product managers, salesmen, our Dutch laboratory and factories. • Reporting products to the Danish “produktregisteret”. • Prepare Certificate of analysis (CoA). • Customer… Show more My responsibilities included • Preparing and update Safety Data Sheets (according to the defined standard of quality). • Labelling control and update. • Responsible for Personal Care products in Denmark meet the Danish regulation. • Support and communication intern to Marketing, product managers, salesmen, our Dutch laboratory and factories. • Reporting products to the Danish “produktregisteret”. • Prepare Certificate of analysis (CoA). • Customer Service. • Responsible for the Laboratory. • Ensure weekly documentation of Carlsbergs washing plant for bottles were following the defined standard of quality. • Prepare Certificate of analysis (CoA). • Receiving incoming reclamations of chemical products, register and analyse for inorganic parameters. • Inorganic analysis off products among others as pH, spectrophotometric determination of minerals, acid/basic determination. • Reporting results to the product managers. Show less

  • LC Groent
    • Freensborg
    • Gardener, freeland/self-employee
      • Aug 2005 - Dec 2006

      My responsibilities included Planning of corps, order seeds, growing vegetables, accounting My responsibilities included Planning of corps, order seeds, growing vegetables, accounting

    • Denmark
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Laboratory Technician
      • Oct 1998 - Sep 2005

      My responsibilities included • Protein bindings studies at plasma from clinical studies. • Work in compliance with GLP. • Handle the planning and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Performed pharmacokinetic and pharmcodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk… Show more My responsibilities included • Protein bindings studies at plasma from clinical studies. • Work in compliance with GLP. • Handle the planning and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Performed pharmacokinetic and pharmcodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk quality. • Refine dosing methods and animal models. • SOP writing and update. • Member of Novo Nordisk Ethic review Committee (ERC).

    • Laboratory Technician
      • Aug 1989 - Sep 1998

      My responsibilities included • Bio analysis on “Cobas”. • RIA (bone markers). • ELISA (bone markers). • Handle the planning and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Performed pharmacokinetic and pharmcodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk quality. • Refine dosing and… Show more My responsibilities included • Bio analysis on “Cobas”. • RIA (bone markers). • ELISA (bone markers). • Handle the planning and documentation of In vivo PK and PD experiments (large animals and rodents) including different dosing methods and operation techniques. • Performed pharmacokinetic and pharmcodynamic calculations in Excel, Prim and Phoenix Pharmaceutical software. • Reporting data according to the defined standard of Novo Nordisk quality. • Refine dosing and animal models. • SOP writing and update. • Work in compliance with GLP.

Education

  • Frederiksborg Statsskole, Hillerød. Laborant skolen, Amager

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