At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

Experience Requirements:10+ years of experience in Regulatory Affairs or other relevant industry experience Degree in a scientific field is preferred.

Specific Job Responsibilities:

Responsible for coordinating regulatory submissions sent to the distributor countries and responsible to prepare submission under the Mexican requirements. Responsible for submissions which may include CMC variations, labeling updates and renewals. Provides regulatory expertise to labeling changes and to submission teams on specified projects and topics.Provides input to senior Regulatory Affairs professionals in the preparation of country specific labeling.May be responsible for ensuring product packaging and associated information is updated and maintained in accordance with the product licenses.Participate in group meetings and local and global product submission team meetings and present project status updates and strategy approaches to moderately complex programs/projects.Responsible under guidance of immediate manager for own self-development and acquisition of required regulatory skills and knowledge.Initiates or contribute to local process improvements which have an impact on the working of the Regulatory Affairs function or other departments.Excellent organization skills and ability to work on a number of projects with tight timelines is required.Excellent verbal and written communication skills and interpersonal skills are required.Must have in-depth knowledge of regulatory requirements in Mexico and some knowledge for Colombia, Argentina, Chile and Uruguay. Work is performed under minimal direction of a senior Regulatory Affairs professional.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.