Manager, Engineering Knowledge Management

Responsibilities: • Responsible for project activities required to scope, develop, procure, construct and qualify new equipment and facilities required to meet facility production throughput demands • Leads multi-disciplinary Teams through project life cycle activities to deliver capacity expansion capabilities to meet global and local strategic requirements • Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval • Project Teams are responsible for completion of project lifecycle activities through turnover to routine commercial production • Responsible for generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for senior site management and Global Steering Committees Qualifications: • MS/MBA/BS/BA in Engineering, Business Administration or Life Sciences preferred or local equivalent • 5+ years practical and leadership experience in pharmaceutical industry including direct management experience in Manufacturing, Engineering or Quality Assurance • Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility • Understanding of project management principles and project lifecycle phases. Knowledge of Validation, CMC and facility regulatory submission requirements Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

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CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.

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