Consultant contract Payment Day rate Requirement EU right to work essential Leap29 is supporting a large-scale energy project...
in more than one standard (i.e. ISO 22716, EU GMP, WHO GMP/GDP, EFfCI and EXCiPACT, ISO 15378, ISO 9001, etc.) and conduct...
and regulations such as MDSAP, ISO 13485 and country and region-specific regulations (i.e. FDA 21 CFR 820, EU IVDD). Qualified...
. Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO...
standards and regulations such as ISO 13485, MDSAP, FDA 21 CFR 820, and EU IVDD. Proficiency with MS Office tools (Word, Excel...
countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU. IntelliPro...
Available Primary focus of this position is to assist R&D EU MDR and Manufacturing related testing, and associated test adjacent tasks...
. This role will also oversee the development of documents to meet EU MDR requirements including clinical evaluation reports... requirements and ensure compliance with ISO 14155, FDA, EU MDR, and other global standards and regulations. · Serve as clinical...
(minimum) Role Location: Fully Remote - must be based in the EU - applications outside will not be considered. The Company...
manufacturing SOPs. Essential Skills Strong knowledge of FDA and EU regulations for APIs and Drug Products. Ability...