Quality Engineer II
preferred with an in-depth understanding of (GMP/QSR/ISO/MDD/MDR) regulations a plus, with focus on inspection points...
preferred with an in-depth understanding of (GMP/QSR/ISO/MDD/MDR) regulations a plus, with focus on inspection points...
medical device regulations such as Part 820, 1271, MDD 93/42/EEC, and ISO 13485:2003. Essential Duties and Responsibilities...
, 1271, MDD 93/42/EEC, and ISO 13485:2003. Essential Duties and Responsibilities Reviews and processes all incoming POs...
to site, division, corporate, FDA, ISO, MDD, MDR and individual country requirements. Driving good manufacturing...
. PNSCR conducts phase II-IV psychiatry trials ranging from MDD, Schizophrenia, Alzheimer's Disease, and Bipolar Disorder...
documentations to support compliance with regulatory requirements. Fulfills selected requirements under the European MDR, MDD, Japan...
/211;ISO 13485, ISO 14971, CMDR, MDD and JPAL is preferred. Solid grasp of computer systems used in a manufacturing...
such as Major Depressive Disorder (MDD), Bipolar Disorder, Schizophrenia, Borderline Personality Disorder (BPD) and Substance...
, ISO 14971, IEC 60601-1, IEC 60601-2-18, FDA and MDD. Experience developing embedded systems with optics for medical...
International Standard, CMDCAS, FDA, and MDD/MDR regulations. We operate the Quality System as an overall management system...