This is what you will do. Alexion’s Product Development and Clinical Supply (PDCS) organization is seeking an expert synthetic organic chemist to lead our strategic capability build in drug substance continuous processing, for deployment across an emerging small molecule portfolio. The Director, Continuous Process Development, will demonstrate deep expertise in flow chemistry to design safe, scalable, and cost-effective synthetic routes, with a s...
Location: Wilmington, United States. Job reference: R-195640. Date posted: 03/22/2024. This is what you will do. The Site Contract Associate Director (SCAD) is responsible at country level for providing leadership, direction, and guidance through process improvement, interactive communication and stakeholder management. The Site Contract Associate Director (SCAD) will support country oversight of the Master clinical study agreement, single clinic...
Location: New Haven, United States. Job reference: R-193624. Date posted: 02/29/2024. This is what you will do. The Associate Scientist II will join the Injectable Drug Product Development team to support the development of Alexion’s bio-therapeutic candidates. This individual will develop injectable formulations with fit for purpose analytical methods, perform analytical testing, and draft reports for the implemented studies. Work independently ...
Location: New Haven, United States. Job reference: R-193973. Date posted: 03/05/2024. This is what you will do. The successful candidate will be a member of the Genomic Medicine Drug Product Development group within Injectable DPD. This individual will have a direct impact on a dynamic and growing group of scientists and engineers developing adeno-associated virus (AAV) based gene therapy products within the larger Alexion Rare Disease Business U...
Location: New Haven, United States. Job reference: R-193630. Date posted: 03/01/2024. This is what you will do. Lead cross-functional efforts in the research, design and execution of scientific studies to enable the drug product (DP) formulation and process development, characterization, commercial validation and regulatory filing of parenteral/injectable biologic products. Lead the development of early and late stage formulation development effo...
Location: New Haven, United States. Job reference: R-193963. Date posted: 03/05/2024. The successful candidate will be a member of the Genomic Medicine Drug Product Development group within Injectable DPD. This individual will have a direct impact on a dynamic and growing group of scientists and engineers developing adeno-associated virus (AAV) based gene therapy products within the larger Alexion Rare Disease Business Unit organization. This tea...
Location: New Haven, United States. Job reference: R-193633. Date posted: 03/01/2024. This is what you will do. Clinical QC Specialist will perform assigned tasks in support of maintaining overall GMP quality and compliance in the Clinical Quality Control laboratory within Analytical Development Quality Control Department. The specialist will help identify and implement quality requirements under the direction of the Senior CQC Compliance Special...
Location: New Haven, United States. Job reference: R-194194. Date posted: 03/07/2024. This is what you will do. The Associate Scientist II will perform assigned tasks to support the operational scale up of Pilot-scale manufacturing processes for Alexion’s bio-therapeutic candidates. Work routinely in collaboration with other members of Process Development and other groups in Product Development and Clinical Supply organization. You will be respon...
Some opportunities happen only once in a lifetime - like a job where you have the chance to change lives. At Alexion, people living with rare and devastating diseases are our Guiding Star. We are driven to continuously innovate and create meaningful value in all we do to help patients and families fully live their best lives. We value the uniqueness and diversity of our employees and recognize that nurturing the diverse perspectives and strengths...
Location: New Haven, United States. Job reference: R-193634. Date posted: 03/01/2024. This is what you will do. The Associate Scientist II will have a primary responsibility for raw data and notebook review across the Clinical QC testing framework ensuring accuracy and compliance for all cGMP activities performed. Additionally, this position offers a secondary opportunity performing assigned experimental tasks and reagent/buffer preparation in Cl...
