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Analytical Development & Quality Control at Siegfried
Analytical Development & Quality Control covers the entire lifecycle of the drug substance portfolio, from the development of methods in projects thru to approval of commercial products. We can offer you far-reaching insights and hands-on experience in all areas of active pharmaceutical ingredient manufacture, from the development of processes and methods through to registration. You are responsible for all analytical aspects of multiple development projects and commercial products across their entire life cycle (excluding drug discovery), through to commercial production and collaborate with Chemical Process Development, Business Development / Sales, Production, Quality Assurance, Registration and Purchasing, as well as interfacing with customers and regulatory authorities, as required. There are plenty of opportunities for project-based collaboration across our facilities in Switzerland, China, the US, Germany and France in connection with tech transfers. Siegfried offers a modern, state-of-the-art workplace, fitted with all the technologies and equipment required to analyze active pharmaceutical ingredients.