Sr. Associate Scientist

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
 

We are seeking a highly motivated, attentive, and self-driven candidate to join our team, Biologics Pivotal & Commercial Formulation and Process Development, as an Sr. Associate Scientist. The successful candidate will contribute to the development of formulation and drug product processes for innovative molecules to advance medicines into the clinic. The candidate will have opportunities for career growth through acquisition of new skills, experiences, and professional relationships in a fast-paced and resource-rich environment. The ideal candidate is expected to be action oriented with high expectations of themselves and others and should possess good verbal and written communication and interpersonal skills.

Responsibilities:

• Design and successfully execute experiments and activities to support formulation and drug process development, including formulation development, Drug Product manufacturing process development, and clinical in-use evaluations. 
• Demonstrate understanding of analytical, biophysical characterization, and process development techniques; lead by example for lab executions. 
• Clearly, timely, and accurately document data in appropriate repositories such as lab notebooks, reports, protocols, etc. following good documentation practices.
• Author technical documents such as protocols, reports, regulatory dossier, etc. and prepare data-focused presentations for internal and external audience. 
• Effectively collaborate with both internal and external stakeholders in project meetings. 
• Analyze data and draft conclusions before discussing with manager or supervisor.Support or represent function and work collaboratively on cross-functional teams to support project team strategy and regulatory filings. 
• Fully embrace a lean-agile mindset, matrix working environment, and continuous improvement.  
• Help support key project or department stakeholders as needed to ensure that company objects are met.
• Support team initiatives to drive business process excellence, scientific innovation, laboratory and work safety, etc.    

Qualifications:

• MS/MA with at least 3 years of relevant experience, or BS/BA with at least 5 years of relevant industrial experience in biologics CMC development. 
• Hands-on laboratory experience required.  
• Experience with formulation development, Drug Product process development, and clinical in-use evaluation for monoclonal antibodies, bispecifics, antibody-drug conjugates, fusion proteins, and other complex biologics formats strongly desired. 

Gilead Core Values 

• Integrity (Doing What’s Right) 
• Inclusion (Encouraging Diversity) 
• Teamwork (Working Together) 
• Excellence (Being Your Best) 
• Accountability (Taking Personal Responsibility)  

The salary range for this position is: $126,820.00 - $164,120.00. 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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Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [email protected] for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

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