Test Validation Lead
Part 11, EU Annex 11, and GAMP 5 guidelines. Proficiency with validation and testing tools: HP ALM/Quality Center, Veeva...
Part 11, EU Annex 11, and GAMP 5 guidelines. Proficiency with validation and testing tools: HP ALM/Quality Center, Veeva...
) of Regulation (EU) 2016/679 (General Data Protection Regulation) as necessary for the purposes of the legitimate interests pursued... of your personal data be restricted. You also have to right to data portability. In addition, you may lodge a complaint with an EU...
) of Regulation (EU) 2016/679 (General Data Protection Regulation) as necessary for the purposes of the legitimate interests pursued... of your personal data be restricted. You also have to right to data portability. In addition, you may lodge a complaint with an EU...
. Experience conducting gap assessments, ensuring alignment with FDA, EU MDR or others global packaging compliance requirements...
. Experience conducting gap assessments, ensuring alignment with FDA, EU MDR or others global packaging compliance requirements...
for complex projects. Working knowledge of ISO 13485 Medical device standards, EU MDD, EUMDR, 21 CFR Part 820 - Quality System...
of blood components being handled, and the necessity to follow all regulatory rules and regulations (AABB, CFR, EU, CLIA, HIPAA...
Documentation (EU) for Medical devices for Regulatory purposes. Manages the compilation of all materials required in submissions...
. Such processing is legally permissible under Art. 6(1)(f) of Regulation (EU) 2016/679 (General Data Protection Regulation... portability. In addition, you may lodge a complaint with an EU supervisory authority. Powered by JazzHR...
) of Regulation (EU) 2016/679 (General Data Protection Regulation) as necessary for the purposes of the legitimate interests pursued... of your personal data be restricted. You also have to right to data portability. In addition, you may lodge a complaint with an EU...