technical documentation and project documentation includingrequirement definitions, functional design specifications and test documentationTrack record of commissioning different plants and lines Experience with peripheral devices commonly used in industrial appliances (nc-drives, presses, distributed I/O
Analyse product deviations and come with solutions - Coordinate and manage project related to Quality Control - Organize and manage internal and external audits - Maintain and improve internal knowledge regarding legislations and food safety standards REQUIREMENTS ...
to change project according to your needs Stable and flexible employment form – you can choose between B2B and permanent contractSelf-development:Technological conferences, eg. Get.NET; internal workshops and trainings; cooperation with local technical groupsSubscription of professional magazines ...
Life Sciences • Minimal 7 years of experience within the Medical Devices industry • Minimal 5 years of experience within Quality Assurance and/or Quality Control • Excellent knowledge of ISO 13485 and ISO 14971 • Broad knowledge of GMP, FDA cfr 820 and CE-marking • An eye for detail and excellent
Devices industry • Minimal 2 years of experience in Quality Control roles • Practical experience with ISO 13485 and Good Manufacturing Practice • Excellent knowledge of European regulations • Excellent communication and writing skills • Fluency in Dutch and English • Extraordinary organizational and
standards REQUIREMENTS • Bachelor of Sciences • Minimal 4 years of experience in the Medical Devices industry • Minimal 2 years of experience in Quality Control roles • Excellent knowledge of European regulations • Practical experience with ISO 13485 and Good
skills & experience in delivery projects, distributed control systems (DCS) and/or programmable logic controllers (PLC), automation engineering and commissioning activities. Process knowhow of Gas Turbines, Steam Turbines and experience related to DCS/PLC TCS systems is considered as a strength. To be
package and the possibility to rete your position in the structure from the beginning.Please note that this is a general description of a new project and the responsibilities based on the experience and development expectations would vary. If you would like to find more details and specific information
communication and interpersonal skills,• Ability to deliver results under pressure,• Ability to work with multiple tasks at the same time,• Microsoft Excel and PowerPoint skills,• Fluent written and spoken English,• PMP or Prince 2 certification in Project Management• Knowledge of project management tool
Control work instructions, assist in the training of value stream personnel in the use of statistical methods, continuous improvements by organizing analysis and problem solving activities for corrective action, provide a clean and organized work environment through 5-S controls. Candidates profile: For our Client we are looking for Candidates for the position ...
process improvements.We are looking for professionals with significant knowledge of Finance & Accounting processes and controls or Audit. Fluency in English and very good knowledge of Spanish, Italian or Germanis also required. Project Managements experience, very good interpersonal skills and the ability
production, quality control, or R&D in a pharmaceutical and/or biotechnology environment with experience in external manufacturing operations or Quality Assurance for external manufacturing - Exposure to regulatory authorities inspections - Deep understanding of Quality processes and systems - Strong plus ...
cabinets, electrical safety for Packaging Equipment is a plus - Can-do attitude - Project Management skills - Disciplined and optimistic mentality - Ability to clearly translate ideas, concepts, and plans - Dutch and English at least at working experience level
implementation of our products in the hospitals, working together with parties in the hospital and external parties together REQUIREMENTS - You have experience in Project Management in the Healthcare industry (3-5 Years) - You are fluent in Dutch and English, French is
bewaarmonsters, dit zijn monsters van grondstoffen en eindproducten: - Controle van aangeleverde bewaarmonsters; - Toezicht houden op het opslaan van bewaarmonster onder juiste omstandigheden (temperatuur, luchtvochtigheid en licht); - In en uitboeken van monsters middels een archiveringsdatabase; - Toezien
documentation. Furthermore, you are responsible for: • Providing advice and support to management in set up of QA/RA processes • Collecting and creating reports of outcomes from audits especially for CAPA’s • Management and control of QMS documentation and reviewing these documents • Taking the lead in