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Manager Regulatory Affairs - RSA AG
Manager Regulatory Affairs - RSA AG, Geneva, Switzerland
Manager Global Regulatory Affairs - Biopharmaceutical CMC
Manager Global Regulatory Affairs - Biopharmaceutical CMC at Boehringer Ingelheim
REGISTRATION PHARMACIST with English and German, Paris/ Lille, France
to sustain LFB products registration in Europe
Corporate Regulatory Affairs Manager
Corporate Regulatory Affairs Manager at Biotest
Cytos Biotechnology Ltd - Regulatory CMC Writer Manager
The primary responsibility is to prepare chemistry, manufacturing and control (CMC) documents for submission to Health Authorities (HA). The employee will participate in Product Development Team meetings to ensure proper communication with the CMC team members for the authoring and compiling of C MC sections for INDs and CTAs. This position requires use of regulatory and technical knowledge related to development, manufacture and testing of Biologics.