5S,8D,Ability to capture relevant adverse event data,Adverse event reporting,APQP,Bids,BOM,BSI,Business acumen,CAD,CAE,Case processing,Castings,Catia,Certification,CFD,CMM,Commercial bid evaluations,Commodity strategy,Compliance,Concept,Containment,Corrective action,Cost reduction,Creo,design,direct,drafting, handling and negotiating,due diligence,environmental,estimating,EU regulatory procedures (CP, MRP, national),expert in ms project / excel,FAIR,FDA submissions,FEA,feasibility,FMEA,franchise marketing,GD&T,global safety database experience,GMS,good pharmacovigilance practice regulations,goods handling,HPRA,indirect,inspection,instrumentation,invoice porcessing,ISO,lean,machined,managing cross-functional areas,materials handling,MHRA,multiple therapeutic areas,negotiation,NPD,NPI,NVH,NX,OBD,oracle,packaging,packaging development,planning and organisation,plastic injection,PPAP,previous drug safety support,problem solving,process improvment,procurement,product registration process,ProE,project managment,prototype,purchase order,purchasing,R&D,reconciliation,Registration Activities,regulatory,regulatory experience in drug development,relationship building,root cause analysis,rotating components,sage,SAP,sheet metal,solidworks,SPC,SQD,SQE,STA,Stastistical process control,Strategic sourcing,Structures,Supplier quality development,Supply chain,Teamcentre,Test bed,Test cell,Validation,Vehicle dynamics,Vendors,Verification,Warranty