Analytical Transfer Manager, ACMC• Coordinate and participate in projects to ensure successful transfer of analytical methods within Novavax and to partners, CMOs in e.g. India, Germany, Czech Rep and Italy.• Manage the activities, and contribute with expertise regarding analytical transfers, in the analytical transfer team.• Coordinate the overall external analytical transfer activities.• Establish necessary routines and work instructions for analytical transfers.

Senior Analytical Scientist, Regulatory and Scientific Affairs• Quality control support for Swedish Match factory analyzes for batch release of smokeless tobacco products globally (Sweden, Denmark and USA).• Supporting the factory laboratories regarding technical, analytical and scientific issues and problems.• Project manager for introducing NIR analysis for batch release of nicotine products at the factories globally.• Responsible for harmonization of analytical methods for pH, moisture, nicotine content and water activity for batch release of nicotine products at the factory laboratories globally.• Leading the method transfer, development, and validation for improvements of the pH and moisture content analysis methods for all Swedish match laboratories.• Project manager of a Six-Sigma project regarding improvements in the routines for weighing samples for analysis.•Taking part in the evaluation of process parameters in the production of tobacco and nicotine products.• Continued work as deputy-QA, responsible for flexible accreditation against SWEDAC and leading the Validation group.

Analytical Scientist, Analytical and Product Science• Six-Sigma Black belt course (23 days during 12 months)- Statistical analysis, tools for root-cause analysis and problem solving.• Project manager of a Six-Sigma improvement project regarding reception and handling of samples.• Quality control support for Swedish Match factory analyzes for batch release of smokeless tobacco products globally (Sweden, Denmark and USA).• Performing statistical evaluations and support the department in such issues.• Continued work as deputy-QA, responsible for flexible accreditation against SWEDAC and leading the Validation group.

Acting Manager, Operations• Acting Manager in a group working with analysis of tobacco and tobacco products in addition to sample registration, sample preparation and reporting of analytical results to customers. • Manage a group of four employees and one trainee.

Analytical Scientist, Chemical Analysis• Project leader for a UHPLC-MS/MS method, which I developed. The method became a recommended method within the international tobacco organization CORESTA. The project included coordination of collaborative studies with labs from all over the world, preparation of study protocols and study reports as well as reporting at international meetings.• Working with international standardization and harmonization of analytical methods within CORESTA.• Responsible for covering new scientific publications and to perform literature searches.• Responsible for the Validation group that supports validation and method development for all the department's methods (GC, LC-MS, ICP-MS, Photometric analysis, FIA, etc.)• Continued work as deputy QA, responsible for flexible accreditation before SWEDAC.• Other: Responsible for literature searches. Chairman of the Method Evaluation Group forum. Member of the quality assurance function (QSF), the Line operations and project forum (VUP). Regularly performance of Internal audits of analysis methods.

Same role and tasks as Nov 2014- Jun 2015

Manager (acting) Chemical Analysis I• Personnel responsibility for five permanent employees, one consultant and one trainee.• Responsible for planning and running the analysis production for all UHPLC instruments (MS/MS, UV and fluorescence). Member of the Chemical Analysis management team.• Other: Recruitment for a permanent position and consultant. Responsible for evaluation and purchase of UHPLC-MS/MS instruments. Chairman of two meeting forums, Method Evaluation Group and Method Development Forum. Involved in preparation and answering questions during an FDA inspection.

Analytical Chemist, Chemical Analysis I• Development and validation of analytical methods for routine use within UHPLC-MS/MS and UHPLC-UV/FLD.• Main responsibility for troubleshooting and problem solving in the routine analyzes for three UHPLC-MS/MS instruments and responsible for operation and maintenance of one UHPLC-MS/MS instrument.• Qualitative and quantitative investigations on UHPLC-MS/MS• Deputy Quality Manager (deputy QA) (from March 2012): Active in the planning and performance of quality enforcing activities like validation of analytical methods, writing and reviewing method descriptions, performing internal audits and preparing supporting material for SWEDAC and FDA.• Responsible for flexible accreditation before SWEDAC (ISO 17025) from September 2013.• Responsible for a Validation group, which supports validation and method development for all the department's methods (GC, ICP-MS, Photometric analysis, FIA, etc.). Also supports method development and validation of methods at the Swedish Match lab in the USA.• Member of the quality assurance function (QSF) and the Line operations and project forum (VUP)• Internal audits of analysis methods.

Method development and validation of analysis methods with HPLC-MS/MS, HPLC-UV (RP to SEC columns) of small (100-300 Da) and larger molecules (300-2000 Da). Also method development of wet chemical analyzes and physical gel characterizations of hyaluronic acid-based gels. Extensive experience of working under GLP/GMP requirements. Instrument responsible for an HPLC-MS/MS-UV instrument.