Sr. Associate II

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
 

Gilead's mission is to discover, develop, and deliver therapies that will improve the lives of patients with life-threatening illnesses

worldwide. As a (Sr Associate I), you are responsible for:

Job Responsibilities

• Supports the technical transfer of new products to site.
• Supports and drives yield improvements on site.
• Supports and/or coordinates internal and cross-functional projects & investigations with limited direction.
• Independently plans and executes assigned experiments or trials that support manufacturing activities and project goals.
• Writes and executes SOP’s, protocols and reports related to process and analytical development.
• Contributes to and may lead technical investigations of process deviations and assessment of their impact on product quality.
• Presents data to applicable departments on the outcome of investigations or optimization activities.
• Seeks areas for improvement/ optimization and leads the execution of these.
• Contributes to and leads technical investigations of process deviations, and assessment of their impact on product quality.
• Defines requirements for, and reviews master batch records.
• Liaises with manufacturing groups to deliver new and improved drug products and processes.
• Can lead one or more specific components of departmental strategic initiatives.

Knowledge & Skills

• Knowledge of scientific and engineering principles in the biopharmaceutical industry.
• Demonstrates excellent verbal, written, and interpersonal communication skills.
• Demonstrates strong computer, organizational, and project management skills.
• Experience working in biopharmaceutical development labs, performing wet chemistry and analytical studies.

Education & Experience

• Bachelor’s Degree with a minimum of four (4) years of relevant experience OR
• Master’s Degree with a minimum of two (2) years of relevant

Preferred Qualifications

• Experience working in an FDA-regulated facility is preferred.
• Experience working in an Manufacturing Science and Technology (MSAT) organization is preferred.

 

The salary range for this position is: $86,275.00 - $111,650.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

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