Jerker Carlsson work email
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Jerker Carlsson personal email
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I am an experienced analytical chemist with more than 20 years in different Analytical Development departments with a well documented GMP and GLP training.I have been a core team member in pharmaceutical projects in pre phase 1 to phase 3, molecules produced synthetically and recombinant, small and large molecules (peptides/proteins). My experience comes from companies with own research and from CMO business.I have performed method development and validation within a large range of analytical technique’s for more than 20 years with most experience from U(H)PLC-UV. I have several years of experience with automated systems for analysis of inhalation devices including method development and validation. I have been assigned specialist roles within LC and MS. I like working with analytical hardware and have been responsible for several equipment and troubleshooting groups. I have worked with a large range of CDS including empower, masslynx, chemstation and chromeleon. I have been responsible of mathematically modulation software in my departments (LC-simulator and Drylab). I have been project manager for technical UHPLC project.I am a broad analytical chemist that prefers to work in an optimistic “can do” environment where we help each other to reach common goals. I also like the possibility to drive my own improvement projects/development activities from start to implementation.
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SpecialistNovo NordiskSkåne County, Sweden -
Manager Analytical DevelopmentIconovo Ab Feb 2020 - PresentLund, Sweden -
Senior Research ScientistNovo Nordisk A/S Jan 2013 - Jan 2020Copenhagen Area, DenmarkMy main responsibility is to support projects with analytical competencies in pre-phase 1 until end of phase 2 and then transfer the project to product supply before phase 3 production. My responsibilities include method transfer/development and validation (phase 1 and 2) of methods for production monitoring and drug substance/product release. I work in close collaboration with the production and characterization department, perform comparability studies, forced degradation, write impurity statements, development reports and drug substance stability protocols/reports. I am responsible of daily planning and prioritizations of my projects activities according to timelines and available resources in our team. I am trained in LEAN with focus on improvement and troubleshooting. I have been responsible for up to 7 projects in parallel.Other responsibilities:Project Manager (UHPLC technical project)CTD (author and expert reviewer of module 3 documents)Equipment/(U)HPLC group responsible (responsible for training, best practice and general support within LC analysis/equipment) Molecules/Techniques: Peptides. Synthetic and recombinant production. (U)HPLC-UV, high resolution MS (limited hands on experience) -
ScientistCmc Biopharmaceuticals A/S Jul 2011 - Dec 2012Working in the Analytical Development (AD) department with biopharmaceutical projects.No day is the other alike! Primary tasks:Transfer of customer methods into AD and internally to QCResponsible of customer project. Direct communication and collaboration with customers.Daily planning and focus on Team workWrite and review analytical reports and SOPsMethod development of HPLC methodsClose collaboration with QC department. -
Senior ScientistAstrazeneca R&D 2003 - Jun 2011Core team member of pharmaceutical projects, supporting with planning, laboratory work (hands-on) and reporting of data. Small molecule projects (inhalation and oral project) in phase 1 to phase 3. I had several responsibilities/special tasks and some of them are listed below:UHPLC: Method development specialist and equipment responsible (support with troubleshooting to other users during implementation of UHPLC).Specialist in advanced Mass Spectrometry. Support to projects with advanced MS analysis i.e. structural elucidations, quantitative analysis of PGIs (potential genotoxic impurities) with LC-MS. Method development and validation with several different techniques, i.e. LC-MS, ICP-MS, CE and HPLC. Introduction of GLP in my department. Stability studies/reports (planning, executing, reporting).
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ScientistAstrazeneca R&D 1998 - 2003Core team member of pharmaceutical projects, supporting with planning, laboratory work (hands-on) and reporting of data.Late phase inhalation projects. Analysis of inhalation devices using Automated systems (Delivered Dose and impactor analsis), HPLC, IR, Solid state analysis (i.e. TAM/DVS), Foreign particles, Method transfer.
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President Of The BoardDraco If 1999 - 2007Draco IF, sports and leisure union within AstraZeneca.5 years as president and 3 years as a member of the board between 1999-2007. About 700 members divided in 20 sections.
Jerker Carlsson Skills
Jerker Carlsson Education Details
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Chemistry -
FolkuniversitetetDanska För Nybörjare
Frequently Asked Questions about Jerker Carlsson
What company does Jerker Carlsson work for?
Jerker Carlsson works for Novo Nordisk
What is Jerker Carlsson's role at the current company?
Jerker Carlsson's current role is Specialist.
What is Jerker Carlsson's email address?
Jerker Carlsson's email address is jc****@****ail.com
What schools did Jerker Carlsson attend?
Jerker Carlsson attended Växjö University, Folkuniversitetet.
What skills is Jerker Carlsson known for?
Jerker Carlsson has skills like Icp, Mass Spectrometry, Hplc, Structure Elucidation, Lc Ms, Method Development, Validation, Gmp, Glp, Chromatography.
Who are Jerker Carlsson's colleagues?
Jerker Carlsson's colleagues are Liliana Patricia Correa Bautista, Txell Arimon, Tareq Abdulrahman, Katarzyna Soltys, Lucia Mastráková, Freja Albjerg Venning, Amanda Deshields.
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