Global MSAT Qualification and Validation Lead – Drug Product

vor 1 Woche


kanton aargau, Schweiz Lonza Vollzeit

This position is located in Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. For Drug Product Services (DPS), our successful Contract Development and Manufacturing Organization (CDMO) branch, located in Stein and Basel, Switzerland we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment Join this outstanding team by applying for this senior position as Global MSAT Drug Product Qualification and Validation Lead What you’ll get: An agile career and a dynamic work culture An inclusive and ethical workplace Compensation programs that recognize high performance What you’ll do: Serve as global process owner for DP manufacturing process control strategy including equipment qualification (PQ), process validation (PPQ), and continued process verification (CPV) for liquid (vial/PFS/Cartridges) as well as lyophilized dosage forms for biological products. Lead the development and governance of corresponding global SOPs, Standards, Templates, and Tools aligned with regulatory and industry best practices. Own the equipment qualification (PQ) strategy for key unit operations e.g. DS thawing, compounding, filling, lyophilization, and crimping. Support customer products throughout the 3 phases of process validation (process design, PPQ and CPV) by providing guidance and oversight to Tech



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