Claire Morris

Quality Control Manager (Chemical Release) at TPI Norway AS
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Contact Information
us****@****om
(386) 825-5501
Location
Kragerø, Vestfold og Telemark, Norway, NO

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Experience

    • Norway
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Quality Control Manager (Chemical Release)
      • Nov 2020 - Present

    • Quality Assurance Associate
      • May 2019 - Nov 2020

    • Quality Control Specialist
      • Jul 2018 - Apr 2019

    • Research and Development Chemist
      • Mar 2016 - Oct 2017

      Method Validation using GC-MS in accordance with ISO17025 Standard.Method development and subsequent validation using UHPLC and HPLC.Incorporate new documents into the Quality Management System (QMS) in accordance with ISO9001, ISO17025 and OHAS18001 standards.Review and approve SOP's, Quality Records, Health & Safety documents etc. as required by personnel and as per the Document Management System (DMS). Method Validation using GC-MS in accordance with ISO17025 Standard.Method development and subsequent validation using UHPLC and HPLC.Incorporate new documents into the Quality Management System (QMS) in accordance with ISO9001, ISO17025 and OHAS18001 standards.Review and approve SOP's, Quality Records, Health & Safety documents etc. as required by personnel and as per the Document Management System (DMS).

    • Analyst on Contract
      • Jun 2014 - Mar 2016

      Represent CLS at various pharmaceutical companies including GSK and Alkermes.Complete routine testing to a high standard in a GMP environment. Work to site specifications and EP specifications. Analysis includes HPLC, GC, FTIR and wet chemistry techniques. Other testing carried out on non-routine basis. Documentation of work and recording of results using LIMS. Method Transfer and investigative analysis performed where necessary. Review and approval of peer work. Represent CLS at various pharmaceutical companies including GSK and Alkermes.Complete routine testing to a high standard in a GMP environment. Work to site specifications and EP specifications. Analysis includes HPLC, GC, FTIR and wet chemistry techniques. Other testing carried out on non-routine basis. Documentation of work and recording of results using LIMS. Method Transfer and investigative analysis performed where necessary. Review and approval of peer work.

    • Entertainment Providers
    • Customer Service Advisor
      • May 2012 - May 2014

      Part time position. Main duties include serving customers, taking and processing bets, manual settling, cash handling and organising events and customer appreciation days. Part time position. Main duties include serving customers, taking and processing bets, manual settling, cash handling and organising events and customer appreciation days.

    • Quality Assurance Student
      • Mar 2013 - Sep 2013

      Completed seven months work placement in the Quality Assurance department. Main responsibilities included reviewing and approving manual batch sheets, updating and monitoring progress of audit response folders and updating risk assessments to ensure compliance with a new QRM System. Completed seven months work placement in the Quality Assurance department. Main responsibilities included reviewing and approving manual batch sheets, updating and monitoring progress of audit response folders and updating risk assessments to ensure compliance with a new QRM System.

Education

  • Limerick Institute of Technology
    Bachelor of Applied Science (B.A.Sc.), Pharmaceutical and Forensic Analysis
    2010 - 2014
  • St. Nathy's College
    2005 - 2010

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