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Consultant-Global Vac Reg Affairs - United States  

Company managed [?] Still accepting applications
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Posted on : 12 August 2017

Project Description

34847
Consultant-Global Vac Reg Affairs
Greenfield
Indiana
United States
Elanco is a global research-based company that develops and delivers product and services to enhance animal health and production. We value innovation, both in scientific research and daily operations, and strive to cultivate a collaborative work environment for more than 7,000 employees worldwide. Founded in 1954, Elanco is a division of Lilly. Our worldwide headquarters and research facilities are in Greenfield, Indiana
  • This role provides global strategic regulatory oversight and is assigned regulatory accountability on vaccine/biopharmaceutical research and development projects.
  • This is accomplished through expert knowledge and understanding of regulations, guidelines, regulatory precedence and the evolving regulatory framework to expedite the research/development and delivery of safe and effective products for animals.
  • To accomplish this purpose, it is necessary for the Consultant to develop, maintain and extend relationships across Elanco components, regulatory agencies, partner companies, industry groups, and academia.
Functions, Duties, Task:
  • Provide leadership of the development and execution of regulatory strategies supporting licensure of new products and claim extensions.
  • Anticipate and resolve key regulatory problems of global vaccine developments.
  • Coordinate and/or conduct the preparation of new biological applications, submissions and responses to questions posed by regulatory agencies.
  • Author and/or review of appropriate policies, SOPs, and guidance documents as needed.
  • Maintain a positive business relationship with regulatory authorities.
  • Align with global, regional and affiliate Regulatory staff to make sure local regulations are met.
  • Work effectively and flexible within all related Elanco disciplines and external collaborators to achieve overall Elanco RA deliverables.
  • Deliver scientifically sound high quality and approvable product submissions.
  • Provide and accept challenge to deliver innovative scientific and regulatory solutions and create innovative culture.
  • Supervise Elanco employees or Contractors and perform appropriate MyPM activities as applicable.
  • Manage project timeline and budget deliverables to facilitate delivery and maintenance of the Elanco pipeline
34847BR
  • Bachelor Degree
  • 10 years experience in research & development and regulatory functions with experience in USDA licensure of biologicals
  • Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.