Martin Andersen Email & Phone Number

Holbæk, Region Sjælland, Danmark

Frederikssund

Head of QC Laboratory

Qbp Laboratoy, Valby

Manager of a team with 10 technicians and 7 chemistsResponsibilities:Daily management in the laboratoryPlanning and allocation of resourcesLEAN – daily board meetingsPreparation of documents (SOPs, user manuals, PM procedures etc.)Approval of analysesQualification of equipment (dissolution, UV spectrometer)Significant results:I was part of a major organizational change, where 3 sections where merged to 2 sections, with reallocation of competences and assignments.

Lumsås

Manager of a team with 15 technicians. Responsibilities:Daily management in the laboratoryPlanning and allocation of resourcesApproval of analysesLEAN – daily board meetingsPreparation of documents (SOPs, user manuals, PM procedures etc.)Review of the analytical part of PQR reports for API and intermediatesQualification of equipment (vacuum oven)Contact to other departments through participation in common board meetings and daily cross organizational follow up. Significant results:With the use of LEAN principles, we reduced lead time in lab significantly and QC went from being a delaying factor to becoming a partner in the overall lead time reduction at the site.In the beginning of 2011 I joined the network group, Netværk Danmark, Management and Development – Sjælland 1.

Hørsholm

Manager of a QC laboratory with 5 employees, 3 chemists and 2 techniciansResponsibilities:Building a GMP laboratory at LifeCycle Pharma for release and stability tests for drug products, in clinical phase I and II. Writing the needed procedures to implement full GMP in the laboratoryQualification of equipment (HPLC and stability chambers) Significant results:The QC laboratory was approved to perform GMP analysis by the Danish Medicines Agency before the company had to change strategy of using own laboratory due to financial issues

Manager in Syntese’s QC laboratory with 8 employees, 1 chemist, 6 technicians and 1 assistant.Responsibilities:Daily management in the laboratoryPlanning and allocation of resourcesApproval of analysesPreparation of documents (SOPs, user manuals, PM procedures etc.)Qualification of equipment including requalification due relocation of the laboratory (HPLC, balances, GC, titrator, heating cupboards)Preparation of the analytical part of PQR reports for APIs and intermediatesRunning the stability program, including writing stability reportsBudget responsibleMember of the leader group, including participation in strategy seminarsSignificant results:Relocation of the QC laboratory from Hillerød to Avedøre Holme. The project was finalized on time, on budget and with no delay in analyses.Successful FDA PAI inspection without any form 483’s related to lab.

Responsibilities: Approval of analyses Qualification of equipment (HPLC) Preparation of documents (SOP’s, user manuals, PM procedures etc.)

Bachelor Of Science (B.Sc.), Chemical Engineering

Laboratory Technician, Chemistry

Matematisk Naturfaglig, Naturfaglig