Director, Regulatory
4 weeks ago
We are currently looking for a Quality Director to join a Global Pharmaceutical company based in Zug, Switzerland. As the Quality Director & QP you will be responsible for supporting clinical products and working closely with CMO’s across various supply chains. Your duties as the Quality Director will be varied however the key duties and responsibilities are as follows:
Oversee all aspects of Quality related to the manufacture and distribution of selected clinical stage products, acting as the Qualified Person (QP) and responsible for product release.
Work closely with the EU registered Qualified Person, ensuring that all drug product batches meet the requirement of the marketing authorisations and or clinical trial applications.
Fulfil the requirements of approved Quality technical agreements with CDMO’s and partners, typically across the US & EU.
To be successful in your application to this exciting opportunity as the Quality Director & QP we are looking to identify the following on your profile and past history:
Currently an operating Qualified Person experienced with Swiss QP regulations and requirements.
Proven industry experience within the Pharmaceutical/Biotechnology sector.
Swiss German/German & English speaking with excellent communication skills.
Qualified Person, QP, Switzerland, Biotechnology, Pharmaceutical, EU, GMP, CMO, CDMO
We look forward to helping you with your next career moves.
We look forward to helping you with your next career moves.
Pharmaceutical, Contract Manufacturing Organisation
Skills: Quality Assurance - Qualified Person - Permanent
Bounds Building, 68 Sackville Street
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