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Niklaus Mehring

Niklaus Mehring

Assistant in the Global Quality Management

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location of Niklaus MehringEttingen, Basel-Country, Switzerland

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  • Timeline

  • About me

    Fascinated in Biotechnology and interested in executing large scale projects in the life sciences industry

  • Education

    • Universität Basel

      2007 - 2009
      Economy and Sustainable Development

    • Universität Basel

      2004 - 2007
      Bachelor Biology

    • Berner Fachhochschule BFH

      2019 - 2020
      CAS Regulatory Affairs

      -Regulatory requirements for medicinal products and medical devices in national and international regulations-Quality and risk management in the pharmaceutical industry with focus on GMP requirements for active pharmaceutical ingredients and drug products-Case study about artificial intelligence in the regulatory area of in vitro diagnostics

    • Universität Basel

      2010 - 2012
      Master's degree Biology, General

      -Bioinformatic analysis of the evolution of telomere associated proteins at the University of Basel-Genetic localization approach in Drosophila with GFP proteins at the National Institutes of Health, Bethesda MD, USA)

  • Experience

    • Actelion (now Janssen Pulmonary Hypertension)

      Jul 2007 - Oct 2007
      Assistant in the Global Quality Management

      -Database management for the information management of internal scientists

    • Viollier AG

      Mar 2008 - Jan 2010
      Laboratory work in Microbiology

      -Preparation of medical probes in the sterile bench on solid and liquid mediums.

    • Novartis

      Aug 2012 - Feb 2013
      Associate Quality Specialist

      -Quality Management with Trackwise AQWA (Corrective and Preventive Actions), archiving and assistant in Health Authority Inspection by Swissmedic-Document Management (ESOPS & TEDI) and Training Management (LMS SPACE)

    • Novartis

      May 2013 - Nov 2019

      -Managed more than 300 External Supply Biologics change projects and ensured timely supply to the markets in compliance with regulatory and cGMP requirements.-Subject matter expert for change control that enjoyed working in several international and cross-funcitonal matrix teams that succesfully ensured the launch and supply for the major biologic products of Novartis (e.g. Lucentis, Xolair and Aimovig).-Black Belt (Superuser) for the Novartis change control system Oracle Agile -Regulatory Compliance Check and remediation of regulatory non-compliances with Quality Assurance.-Implementation of the Regulatory Compliance Check with external suppliers

      • Site Change Coordinator

        Nov 2015 - Nov 2019

      • Junior Quality Expert

        May 2013 - Oct 2015

    • Agilent Technologies

      Mar 2020 - now
      Enterprise Implementations Project Manager

      -Leading contract deployment for large customers in accordance with defined project plans in crossfunctional and international Matrix Teams (Program management, Service Sales, Service Delivery, Inventory management, Customer Operations and Supplier Management)-Implemented Laboratory Asset Management projects in the last four yours in Switzerland, Austria, the Netherlands and Germany (Roche Basel RAMP, Novartis Tirol LISA, Sanofi LAMM Amsterdam and Boehringer Ingelheim Clamp)-Data management of laboratory asset inventory lists-Managing customer communication on all levels (Project Managers, Lab Engineers& Scientists, Procurement and Management) including customer expectations, issues and feedback-Solving a broad range of problems involving multiple departments and external customers-Project Management and Governance of large Relocations in Switzerland, Austria and Germany Show less

  • Licenses & Certifications