Manufacturing Engineer
keeping, communication, and documentation practices. Support compliance for GMP, ISO 13485:2016, MDD/MDR, and safety...
keeping, communication, and documentation practices. Support compliance for GMP, ISO 13485:2016, MDD/MDR, and safety...
and presentations. A working knowledge of GMP, ISO 13485 & MDD requirements. Requisition ID: 599496 The anticipated annualized...
(such as ISO 9001/13485, FDA 21 CFR part 820, and IVD/MDD directives). Serve as the primary representative for software quality...
and presentations. A working knowledge of GMP, ISO 13485 & MDD requirements. Requisition ID: 599496 The anticipated annualized...
management, including FDA QSR, MDD, EU MDR, CMDR, ISO 13485, ISO 14971, and Philips procedures. Ensure the systematic...
of results, and generate detailed technical reports. Provide support to project teams in the compliance of ISO13485, MDD / MDR...
in medical device/pharma industry. Experience to include ISO 13485, 21 CFR 820, MDD 93/42/EEC, EU MDR 2017/745, and MDSAP...
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...
International Standard, CMDCAS, FDA, and MDD/MDR regulations. We operate the Quality System as an overall management system...