Senior Principal Engineer, Human Factors

Act as Lead Human Factors Engineer Plan and execute Human Factors Engineering activities in drug delivery device projects, including development of secondary packaging and Instructions for Use Set and drive best practices within DDS&P; for Human Factors Engineering Support standardization of approaches for Task Analysis, Use Risk Assessment, and other key deliverables Lead HF oversight of secondary packaging development Partner with project leads and the cross-functional development team on planning and execution of projects Lead development of selection criteria and evaluation of the user interface for new products Collect, maintain, and utilize data on user capabilities and known use problems with combination products Contribute to the development of Company Core Data Sheets (CCDS) Plan and execute Formative and Summative evaluations, including selection and oversight of CROs Leverage existing data to support regulatory submissions, e.g., comparative analysis Develop dossier submissions for HF content, including HFE/UE Report, and responses to regulatory agency questions Monitor industry trends, standards, and regulatory guidance

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

• Excellent communication skills and a track record working in a matrix environment

• Ability to influence and promote a culture of continuous improvement

• Subject Matter Expertise on: IEC 62366 family of standards and related regulatory guidance, User Capabilities – anthropometric basis, Use Risk Assessments

• Proven track record of: Evaluation of user interfaces for drug delivery devices, Development of instructional materials for product labelling and artwork

• Relevant academic qualification in an appropriate field, e.g., Ergonomics, Psychology or a suitable Science or Engineering degree

• At least 8 years of related experience in the pharmaceutical or medical device industry

• Ability to travel internationally up to 20%