Started in 2015 as a Bioassay Associate Scientist. My main area of expertise currently are Host Cell Protein (HCP) process impurities. Strong focus on method and platform validations, matrix verifications, vast experience in the ELISA method. I am also a proficient Tecan specialist, which involves method transfers, handling crashes and breakdowns. I have been using this piece of automation for the last 5 years and attending training in the UK. Lastly I have been involved in several method… Show more Started in 2015 as a Bioassay Associate Scientist. My main area of expertise currently are Host Cell Protein (HCP) process impurities. Strong focus on method and platform validations, matrix verifications, vast experience in the ELISA method. I am also a proficient Tecan specialist, which involves method transfers, handling crashes and breakdowns. I have been using this piece of automation for the last 5 years and attending training in the UK. Lastly I have been involved in several method validations on our numerous cell based bioassays. Outside of the lab space, I have also been a Stability Lead for early phase products, this involves ensuring the testing campaign runs smoothly. I am currently the AD lead for Continuous Improvement, this involves providing yellow belt training, promoting the culture of lean and encouraging savings. Show less

Manufacture of media products in a level 5 clean-room environment as per SOP, involving mixing, filtration and dispensing, involving extensive use of SUT, (Single use Technology)Magnetic particle coupling, coating magnetic particles with amino dextran.In process testingComplete daily monitoring, calibration and maintenance of equipmentParticipate in continuous improvement projects using lean and 6 sigmaMaintain accurate and detailed recordsInitiate NCR investigations and… Show more Manufacture of media products in a level 5 clean-room environment as per SOP, involving mixing, filtration and dispensing, involving extensive use of SUT, (Single use Technology)Magnetic particle coupling, coating magnetic particles with amino dextran.In process testingComplete daily monitoring, calibration and maintenance of equipmentParticipate in continuous improvement projects using lean and 6 sigmaMaintain accurate and detailed recordsInitiate NCR investigations and create CAPATraining new staff members in all aspects of manufacturing Show less

Digestion of specific methodsCalibration and maintenance of equipmentTraining new staff members in digestion methods

Manufacture of Clinical Chemistry Reagents as per GMP manufacture protocol, involving extensive use of SUT.In-process testing to required specificationsCalibration and maintenance of production equipment, including ph meters, densitometerFailure investigation where required on non-conforming product/OOSUpkeep of neat accurate written records as per relevant Formulation SOP’sMaintenance of Housekeeping/Safety/Environmental standardsCompliance of regulations both FDA and… Show more Manufacture of Clinical Chemistry Reagents as per GMP manufacture protocol, involving extensive use of SUT.In-process testing to required specificationsCalibration and maintenance of production equipment, including ph meters, densitometerFailure investigation where required on non-conforming product/OOSUpkeep of neat accurate written records as per relevant Formulation SOP’sMaintenance of Housekeeping/Safety/Environmental standardsCompliance of regulations both FDA and ISO Show less

▪ Cell passaging, cell revival and creating cell banks, including plating, counting and staining▪ Was responsible for the growth and maintenance of several different cell lines.▪ Upkeep of neat accurate written records as per relevant SOP’s.▪ Compliance with regulations both FDA and ISO.