Director, RA Global Regulatory Strategy
strategist in two or more major regions in addition to the US, such as EU or Japan. Strong global drug development foundation...
strategist in two or more major regions in addition to the US, such as EU or Japan. Strong global drug development foundation...
: Knowledge of applicable regulations and standards affecting Oncology Pharmaceutical Products in key markets of US, EU and JP...
but not required. Knowledge of applicable regulations including, but not limited to, 21 CFR 803, 21 CFR 820, 21 CFR 821, 21 CFR 4, EU Medical...
to the US, such as EU or Japan. Strong global development foundation with business acumen. Note: Higher education may...
13485, ISO 14971, 21 CFR 4, 21 CFR 820, EU Regulation 93/42/EEC (MDD) & 2017/745 (MDR) Able to travel up to 10% of the time...
Fundamental knowledge of Medical Device Design Control (DHF, EU MDR, CE Mark) Strong data analysis skills and experience (Minitab...
collection and processing of personal information from individuals who live in the European Union (EU)....
of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment...
of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment...
of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment...