Kristin Hronn Thorbjornsdottir

Project Manager at Coripharma
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Contact Information
us****@****om
(386) 825-5501
Location
Hafnarfjörður, Capital Region, Iceland, IS

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Experience

    • Iceland
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Project Manager
      • Aug 2018 - Present

      Transfer of new products to the site, including preparation of Manufacturing Instruction, Manufacturing Support, Process Validation and Support to Clients. Serialization implementation Project management of various projects. Preparation of Risk Assessments for various projects. Transfer of new products to the site, including preparation of Manufacturing Instruction, Manufacturing Support, Process Validation and Support to Clients. Serialization implementation Project management of various projects. Preparation of Risk Assessments for various projects.

    • Assistant Head Pharmacist
      • May 2017 - Aug 2018
    • United States
    • Pharmaceutical Manufacturing
      • May 2010 - Apr 2017

      In 2010 I took on a new department within manufacturing responsible for scale up from R&D, improvements of products, manufacturing support for validation batches and transfers to other Actavis sites. In 2013 process- and cleaning validation were added to the responsibility of the department with increased responsibility and number of employees. The department had seven specialists and apart from running the department from day to day basis I also participated in professional projects within the department as well as with other department. Alongside my job as a manager I have taken on other roles for example participating in SAP project on behalf of manufacturing, teaching in an in-house pharmaceutical school and global project management for transfer projects due to the closure of the site in Iceland. Show less

      • Sep 2002 - May 2010

      See role of department below. Started as a specialist and then became a manager. This was a department of 17 employees.

      • Mar 1998 - Sep 2002

      Key responsibilities:Preparation of manufacturing instructions and standard operation procedures for tablet manufacture and packaging, deviation investigation, improvements on products and processes, participation in internal and external audits and transfer of products to other Actavis manufacturing sites.

    • Analyst
      • Jun 1997 - Mar 1998

      Analytical work on illegal drug substances and alcohol tests. Analytical work on illegal drug substances and alcohol tests.

Education

  • Háskóli Íslands
    Master's degree, Pharmaceutical Sciences
    1992 - 1997
  • Fjölbrautarskólinn í Breiðholti
    Stúdentspróf, Náttúrufræðibraut
    1988 - 1991

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