quotation and technical implementation process.- Maintain an in-depth understanding of connectivity requirements, current clinical practice and products/technologies.Requirements- Bsc in IT/Networking- At least 3 years exposure to sales positions, preferably Electronic Monitoring Records related- Fluent in
week/maand.Requirements- HBO werk en denkniveau richting bedrijfskunde, operationeel management. - 3-5+ jaar relevante werkervaring in een soortgelijke leidinggevende functie.- Uitstekende kennis van IT systemen. - Kennis van chemie is een pré. - Uitstekende kennis van de Nederlandse en Engelse taal in woord en
looking for an Operations Manager.Location: Uithoorn, the NetherlandsResponsibilitiesKey responsibilities Supervising, coordinating, and monitoring all activities in Production and the Quality Service Group in such a way as to ensure that the manufacturing process is realised within the scheduled time in
organise cell production and reaching the GMP production target. Manage the team in executing production process in dedicated manufacturing area. Interact with development manager on required improvements to the production process. Analyse results, write reports and provide management information like
doel de vooropgestelde targets (savings) te behalen • streven naar ‘optimal total cost of ownership’ • fungeren als Category Manager Indirect Spend: • handelen als relatiemanager tussen de diverse afdelingen ( Site & Maintenance Managers, IT, Marketing, HR,... ) en de potentiele leveranciers ...
er al meer dan 85.000 artikelen in onze webshop en wordt dit aanbod dagelijks uitgebreid. Ons bedrijfspand heeft naast kantoorruimte, meer dan 10 magazijnen, waaronder 3 palletmagazijnen met een capaciteit van 2.000 pallets.Role DescriptionSamen met je collega’s van de IT afdeling, bestaande uit 3
Clinical-stage company and Immuno-Oncology/Cell Therapy. Glycostem is looking for the experienced Clinical Trial Manager to monitor the pan-European clinical development in Immuno-Oncology, reporting directly to the Senior Vice President Clinical Affairs. ResponsibilitiesThe basic responsibility is to execute
entire supply chain. You will be examining the current supply chain and initiate new initiatives to improve the overall efficiency of the processes.ResponsibilitiesYou will be responsible for analyzing and improving the logistical processes within the supply chain. It will be your job to make the
organisation, based in Netherlands.The CompanyIf you’re seeking a career where you can truly make a difference in the lives of others, where you can work at the forefront of biotechnology with the top minds in the field, you’ll find it at this international pharmaceutical company with the European distribution
your expertise in a way that makes an impact.Role DescriptionThe Functional Application Manager configures and maintains manufacturing workflows in SAP/MES according to the excellence standards and acts as Functional 1st line support in P2FG MES related questions. Act as process and systems custodian ...
organisation, based in Noord-Brabant Netherlands.The CompanyIf you’re seeking a career where you can truly make a difference in the lives of others, where you can work at the forefront of biotechnology with the top minds in the field, you’ll find it at this international pharmaceutical company with the European
unique and life-saving Medical software. As QA/RA Manager you are responsible for the quality assurance and regulatory affairs strategy at a fast-growing medical device start-up. This concretely means further setting up a quality management system (ISO 13485), defining a regulatory strategy concerning
results and controlling the laboratory performance in a GMP environment? Is a laboratory more than a room with equipment ? As Quality Control (QC) Manager in Gorinchem we offer you the opportunity to provide highly reliable QC data in timely manner and in line with production schedules and quality
organisation, based in Noord-Brabant Netherlands.The Company.Role DescriptionYou manage and control the category ‘Indirect goods & services’ (IT, Energy, HR, maintenance, waste, R&D, fleet, production & administration, ...)Responsibilities- You execute a structured sourcing model with focus on business needs
Netherlands nearby Amsterdam. Our client is looking for a QA Manager that is responsible for managing quality aspects at external Contract Manufacturing Organizations.Role DescriptionWhat you are going to do...As QA Manager you will be responsible for the products for the EU market for our client. Because you
do it together"Requirements• Experience of quality in a pharma environment• Wide knowledge about GMP, GDP and ISO 9001• Experience in equipment and process validation• Verbal and written fluency in Dutch and English languageAre you interested and do want to apply for this role, please fill out your
Corbion Central R&D and Innovation Centre.ResponsibilitiesAs our new QA Manager Pharma you report to the Manager QA / QC within our Operations Team. As our QA Manager Pharma you are mainly responsible for typical and non-typical quality matters of the Corbion plant, where we have 150 ...
do it together"Requirements• At least 5 years of experience of quality in a pharma environment• Wide knowledge about GMP, GDP and ISO 9001• Experience in equipment and process validation• Verbal and written fluency in Dutch and English languageAre you interested and do want to apply for this role ...