Natasa Liderfelt (Kupres)

Vice President Europe at Optinova
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Location
Greater Uppsala Metropolitan Area, SE

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EvaStina Berger

Jag har både arbetat med Natasa som kollega på Pfizer och som chef på Semcon. Natasa är kompetent och professionell i sin roll som chef och samtidigt en trevlig kollega. Hon har en förmåga att lyssna in och förstå vad kunderna efterfrågar vilket gör henne till en duktig förmedlare av konsulttjänster. Får jag tillfälle tar jag gärna hjälp av Natasa och hennes team!

Lotta Brynö

Natasa är en positiv och energisk tjej som jag gärna rekommenderar för processutvecklings- eller projektledningsuppdrag. Hon är duktig på att driva aktiviteter på ett strukturerat och målmedvetet sätt, är pragmatisk och idérik och har lätt för att samarbeta.

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Experience

    • Belgium
    • Construction
    • 1 - 100 Employee
    • Vice President Europe
      • Aug 2023 - Present

      Working in a global environment with colleges from more than 10 countries. Responsible for sales areas Europe (+26 MEuro), general manager for 2 sales offices in Sweden and Germany with responsibilities of Sales Managers, Finance and Customer Service.Main responsibilities building and growth sustainable businesses and relationships with new and existing accounts within Industrial and Medical segment for fluoropolymer extruded components.My strengths are to build new relationships externally and internally, coaching employees to develop their next level, create innovative working environment, build sustainable work place. Show less

    • CEO Optinova Germany
      • Aug 2023 - Present

    • Finland
    • Plastics Manufacturing
    • 1 - 100 Employee
    • CEO Optinova Nordic AB
      • Apr 2020 - Present
    • Vice President of Sales for Northern Europe (UK, Ireland and Nordic country)
      • Apr 2020 - Aug 2023
    • Sweden
    • Information Technology & Services
    • 700 & Above Employee
    • Area Manager/Department Manager
      • Mar 2016 - Apr 2020

      Departement manager responsible for two departements: Uppsala-Gävleborg and Dalarna. Businesses within Life Science, Energy and Industry.

    • Sales Manager
      • Mar 2012 - Apr 2020

      Engineering, Project management and Quality Services within Life Science, Product Development, Energy and Nuclear businesses.

    • Manager
      • Feb 2014 - Feb 2016

    • Project Manager
      • Apr 2010 - Apr 2012

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Consultant, Process Developer/Project Manager
      • Nov 2012 - Dec 2012

      Coaching in Process Development activities. Coaching in Process Development activities.

    • Sweden
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Consultant, Project Manager
      • Jun 2011 - Aug 2012

      Project leader for upscale activities during development of sublingual tablets, i.e coordinator of Quality by Design (QbD) and packaging activities. Project leader for upscale activities during development of sublingual tablets, i.e coordinator of Quality by Design (QbD) and packaging activities.

    • Consultant, Process Developer
      • Oct 2010 - Jul 2011

      Coordination of project: Cleaning validation (CIP), Process Developer. Coordination of project: Cleaning validation (CIP), Process Developer.

    • Consultant
      • Apr 2010 - Oct 2010

      Installation and PW validation (such as prestudies, PQ, PV). Working also with cleaning issues. Installation and PW validation (such as prestudies, PQ, PV). Working also with cleaning issues.

    • Process Developer
      • Sep 2007 - Mar 2010

      Project and validation manager for investment, process improvement and cleaning validation projects. Requirement handling including validation document and traceability matrices. Technical expert on new equipment purchased by Q-Med for production under QSR/GMP. Project and validation manager for investment, process improvement and cleaning validation projects. Requirement handling including validation document and traceability matrices. Technical expert on new equipment purchased by Q-Med for production under QSR/GMP.

    • Events Services
    • 1 - 100 Employee
    • Process Developer
      • Apr 2003 - 2007

      Responsible for sterile process of equipment/product including: all qualification activities, responsible for inspections by authorities (Swedish medical agency and FDA), deviation investigation etc. Six Sigma greenbelt project manager and assistant project manager for a large production project.

    • Process/Quality Engineer
      • Mar 2001 - Apr 2003

      Pharmacia, Aseptic manufacturing, Process and Quality EngineerResponsible for change control, deviation investigation. Participate during authority inspections (e.g. FDA), implement instructions for vision system and educate personnel on SOP:s

    • QA Release
      • Mar 2000 - Mar 2001

    • Wholesale Drugs and Sundries
    • Laboratory Engineer
      • 2000 - 2000

Education

  • Mälardalen University
    160 p, Biotechnology
    1996 - 2000

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