On any given day you will be responsible for:
Communicating and explaining the quality system both inside and outside the organization (i.e. to suppliers)
Initiating and organizing the implementation of actions after abnormalities have occurred so that (similar) abnormalities can be prevented
Motivating, encouraging, coaching, and influencing new behavioral patterns both within the internal organization and at suppliers
Operations responsibilities:
·Adhere and ensure conformance to all Internal Quality procedures
·Identifying, handling, and coordinating containment actions after articles have been produced either internally or externally that do not comply with the specifications
·Drawing up and analyzing investigation and control results and the distribution of reports
·Formulating measurement plans and 3D measurement programs
·Suspending production and freezing stock if abnormalities are discovered
·Verifying faults and abnormalities and determining the level of non-conformity
·Carrying out incoming inspections, stock inspections, process inspections, and end product inspections
·Verifying faults and abnormalities and determining the level of non-conformity
·Carrying out tests and measurements: Carrying out incoming inspections, stock inspections, process inspections, and end-product inspections
·Ensure calibration equipment standards are maintained
· Following international quality ISO 9001 -2015 Standard
·Monitor and carry out Marel standard procedures when supplier discrepancies are identified
·Provide support as required in the improvement of quality-related processes
·Participation in internal and external quality consultation meetings and improvement projects
·Demonstrate continuous performance of duties according to Marel HSE standards and policies
·Assist in root cause analysis, process mapping, etc. to make incremental changes to process and procedures