...health. We operate in an international environment and value teamwork and excellence. More information about Krka Belgium at: JOB DESCRIPTION:After a thorough introductory training followed by follow-...
...health. We operate in an international environment and value teamwork and excellence. More information about Krka Belgium at: JOB DESCRIPTION:After a thorough introductory training followed by follow-...
...medical imaging, and surveillance. You will have the unique opportunity to shape the future of our product offerings and contribute directly to our mission of revolutionizing the imaging technology se...
...medical guidelines. H&O Equipments is the driving force behind countless successful treatments worldwide. The company sets high standards and defines the benchmark for cryosurgical precision. Its ambi...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...medical device manufacturing or a related industry, with 5+ years in a Quality Auditing function preferred. Working knowledge of Medical Device Regulations/In Vitro Diagnostic Regulation, cGMP, CFR 82...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...
...Medical Device Single Audit Program, and other international regulations. Experience with automotive PPAP is a plus. Industry Experience: 5+ years’ experience in medical device manufacturing or a rela...