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As our new Associate Director RA Device, you will be driving the regulatory strategy for device constituent parts of combination products and use your device regulatory experience...
Monitor and analyze the impact of emerging or revised laws, regulations, enforcement actions and other changes that impact the manner by which the clients' products are regulated...
You will be responsible for leading global, complex extractables and leachables (E&L) projects with internal and external laboratories. You will work with site and global teams to...
Ensuring clinical studies are conducted according to the study protocol, SOPs, ICH/GCP regulations, and study-specific manuals and procedures; Participating in the development of...
Play a key scientific role in multiple projects in the field of preclinical/clinical biomarkers in (immuno)oncology by participating in cross-functional biomarkers projects....
As Manager, DMPK and PK/PD Modeling, you will lead our Drug Metabolism and Pharmacokinetics (DMPK) activities. In this role you will have the opportunity to develop scientific...