Responsibilities:- Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals needed to conduct current and future business activities; and produce, sell, and distribute its goods and services. - Support development of consistent roles and work processes. - Oversee development of plans, cost estimates, and schedules. Acquire the necessary permits and approvals. - Monitor regulatory developments and advise management on the potential impact of regulations on the organization. - Establish and maintain positive relationships with government agencies and other regulatory authorities. - Represent the organization in matters before regulatory, legislative, or industry standards agencies so the organization's interests are advanced. - Prepare materials for legal counsel or external consultants.- Create and compile of registration application documentation.- Regulatory system, data entry and maintenance in/of regulatory systems.
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. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.
