Successfully lead downstream departmental manufacturing resources to deliver on customer commitments and expectations. This means being responsible for the carrying out a variety of functions related to Downstream Biopharmaceutical Manufacturing including but are not limited to activities such as conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. Ensure right the first time and on time delivery of protein purification processes to support clinical and commercial biologics manufacturing. Demands are to be met in accordance with established safety, quality, efficiency, and regulatory standards. Lead all aspects of all manufacturing resources including personnel and equipment. Operate cross functionally and collaborate with peers both within and outside of department. Successfully drive focused performance management and talent development of direct and in-direct reports. Demonstrating proactive leadership inside of the department and strategic delivery of company goals and a continuous improvement approach is also an expectation.
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Job Type
Full-time
Career Level
Manager