36 Eu Mdr Jobs

d cad / solidworks eu mdr medical device tolerance analysis mechanical design iso material selection assembly design mechatronics 3d cad product design root cause

quality management regulatory compliance process improvement corrective actions technical problem solving h1

quality management regulatory compliance process effectiveness cross functional collaboration corrective actions healthcare metrics sdlc

regulatory compliance quality management cross functional collaboration regulatory documentation ivd knowledge workforce wages compensation interview

systems engineering verification & validation risk management requirements engineering system design h1 interpersonal skills

regulatory affairs leadership quality management systems cross functional collaboration product validation compliance regulatory documentation monitoring iso 13485 capa

electrical circuit design medical device compliance eda tools proficiency technical leadership problem solving electrical engineer senior electrical engineer mitigation engineering iec electrical engineering electrical safety electrical design

electrical circuit design medical device compliance eda tools proficiency technical leadership problem solving electrical engineer senior electrical engineer mitigation engineering iec electrical engineering electrical safety electrical design

clinical evaluation expertise medical writing proficiency literature review skills data analysis ability regulatory knowledge understanding regulatory affairs clinical trials clinical operations biostatistics process development medical affairs clinical research

" [ "cybersecurity strategies" "scripting automation" "security tool integration" "risk management" "vulnerability management" ] " ceh cissp security design ethical hacker cloud security director

systems engineering requirements engineering risk management verification & validation system design interpersonal skills

scripting automation cybersecurity strategies risk management cloud security security protocols ceh cissp security design ethical hacker director vulnerability management

internal auditing techniques fda regulatory knowledge capa process management iso standards expertise quality metrics analysis des scheduling manufacturing implementation cgmp process data

cad proficiency gd & t expertise design control risk management tolerance analysis mechanical engineer documentation nx failure analysis solid edge

quality assurance principles fda compliance standards iso regulations process improvement methodologies audit management experience enhancements scheduling manufacturing lean 5s innovation implementation harness

prisym labeling solutions label design management regulatory compliance understanding process automation knowledge multi site label management supply chain

quality management system root cause analysis internal audit expertise regulatory compliance team leadership complaint handling suppliers iso 13485 customer complaints oos product quality supplier audit capa quality assurance quality standards

regulatory submissions quality assurance technical documentation risk management cross functional collaboration iso 13485

regulatory compliance product testing document preparation analytical research cross functional collaboration amp environmental compliance product compliance supervision product development manufacturing mechanical engineering implementation

complaint investigation quality management medical device risk project management stakeholder communication complaint handling iso 13485 customer complaints customer quality

regulatory expertise risk benefit analysis documentation compliance post marketing surveillance advanced pc skills regulatory requirements regulatory affairs

quality assurance expertise customer complaint handling post market surveillance medical device regulations root cause analysis customer complaints capa customer quality quality tools

quality management system regulatory compliance process effectiveness cross functional collaboration problem solving techniques h1

packaging design material qualification regulatory compliance cad software project management iso manufacturing packaging engineer documentation dfm ideas dfmea engineering change management production amp supervision innovation implementation prototype printing plm creo

packaging design material qualification project management cad software documentation management iso manufacturing packaging engineer dfm ideas dfmea engineering change management production amp supervision innovation implementation prototype printing plm creo

quality management regulatory compliance problem solving process effectiveness cross functional collaboration healthcare metrics sdlc

quality management system regulatory compliance corrective actions process improvement cross functional collaboration capa quality assurance

packaging design material qualification project management cad software proficiency good manufacturing practices iso packaging engineer documentation dfm ideas dfmea engineering change management production amp supervision innovation implementation prototype printing plm creo

packaging design cad software project management quality standards material testing iso manufacturing packaging engineer documentation dfm ideas dfmea engineering change management production amp supervision innovation implementation prototype printing plm creo

medical writing expertise regulatory knowledge data analysis skills literature review communication skills conference database

quality management system regulatory compliance process improvement corrective actions cross functional collaboration healthcare metrics sdlc

medical writing expertise clinical evaluation reports literature review skills data analysis proficiency regulatory knowledge conference database

design quality engineering risk management expertise software verification fda compliance cross functional collaboration conference software design software engineering

quality engineering support risk management expertise software verification skills fda regulatory compliance cross functional collaboration iso 13485 statistical tools qa iso 9001 validation minitab pfmea process validation ts

quality engineering support design controls application fda submission guidance software verification activities risk management expertise iso 13485 statistical tools qa iso 9001 validation minitab pfmea process validation ts

design quality engineering regulatory compliance risk management software verification agile methodologies iso 13485 statistical tools qa iso 9001 validation minitab pfmea process validation ts