Bas Van Der Lee
About
Bas Van Der Lee is from Haarsteeg, North Brabant, Netherlands. Bas works in the following industries: "Biotechnology Research". Bas is currently Sr. Manufacturing Process Speciaist at Dynavax GmbH, located in Düsseldorf en omgeving. In Bas's previous role as a Manufacturing Process Specialist at Dynavax Europe, Bas worked in Düsseldorf en omgeving, Duitsland until Jan 2020. Prior to joining Dynavax Europe, Bas was a Cross Sector Improvement engineer at YER and held the position of Cross Sector Improvement engineer at Veldhoven. Prior to that, Bas was a Process specialist at Dynavax GmbH, based in Düsseldorf from Oct 2016 to Feb 2017. Bas started working as Manufacturing Process Specialist at The Janssen Pharmaceutical Companies of Johnson & Johnson in Leiden in Jun 2015. From Jun 2012 to May 2015, Bas was Technical Specialist at The Janssen Pharmaceutical Companies of Johnson & Johnson, based in Leiden. Prior to that, Bas was a Senior Technician at The Janssen Pharmaceutical Companies of Johnson & Johnson, based in Leiden from Jan 2011 to May 2012. Bas started working as Docent scheikunde at Christelijk Lyceum Apeldoorn in Apeldoorn in Sep 2007.
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Bas Van Der Lee's current jobs
Bas Van Der Lee's past jobs
- Deviation lead for site deviations which includes investigation, writing and CAPA definition - Change control / project lead lead for improvements within the manufacturing department - Successfully defended site deviations in the 2018 German health inspection and 2019 FDA inspection - Internal trainer for “Investigator skills” and “Technical writing” workshops - Asset owner of the Material Management System - Data mining / Technical writing / Change controls / CAPA’s / CPV - Bringing Quality Assurance and Manufacturing together - User acceptance testing of a new eQMS system
Cross Sector Improvement engineer
Process specialist Main responsibilities - RCA investigation - CAPA's - Change controls
Part of the process team for the Ad26Zebov/PER.c6 facility at Janssen Biologcs in Leiden. Responsibilities - Selection and purchasing of process equipment - Commissioning of equipment - Development of documentation strategies - Establishing a global standard for closed filling by engineering a closed filling system for drug substance
Part of the upstream Centre of Expertise group which implements changes to equipment and production processes. Responsibilities - Standardization of local and global production processes - Pre-Culture Process improvements - Execution of change controls - Data analysis and reporting - Process equipment ownership - Review/Write technical reports/protocols - Review CAPA/Deviation and change control text - Trouble shooting and problem solving
Part of the upstream Centre of Expertise group which implements changes to equipment and production processes. Responsibilities - Data mining - Perform data trending of process parameters - Update WI/SOP's - Write technical reports/protocols - Trouble shooting
Worked as a part-time teacher during my chemistry master (HAVO4/VWO4/VMBO2)