Associate Director Eu Regulatory Cmc Switzerland
vor 1 Tag
**What your profile should include**:
Experience in CMC regulatory affairs for biological/biotechnological products as an advantage.
Understanding and interpretation of complex scientific issues across projects and therapeutic areas of responsibility as it relates to regulatory requirements and strategy.
Advanced scientific degree (Bachelor of Science, Bachelor of Arts accepted based on experience.
Considerable experience within the pharmaceutical industry and including direct experience in CMC regulatory affairs in development and post-marketing phases for medicinal products.
Experience in Medical Device regulation as an advantage.
Strong expertise in the EU region
Experience managing relationships with CROs and/or contractors are also preferred.
If you are not available but you know someone that would be interested, please forward this to them and help the people in your network. Receive 200 euros for every successful referral.
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