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Gilead Sciences

Sr Scientist, Process Development

Posted 12 Days Ago
Be an Early Applicant
In-Office
Foster City, CA, USA
154K-219K Annually
Senior level
In-Office
Foster City, CA, USA
154K-219K Annually
Senior level
Lead and mentor staff in downstream process development for biopharmaceuticals. Design, execute, and transfer purification processes while driving new technology implementation and contributing to regulatory submissions.
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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
 

Key Responsibilities

  • Lead, mentor, coach, and develop technical staff within and outside the group in all aspects of downstream process development, including protein purification, bioconjugation (antibody-drug conjugates), and new technology implementation.

  • Design and execute experiments to develop efficient, effective downstream purification processes using multiple chromatography modes, filtration technologies, and ultrafiltration/TFF.

  • Drive new technology development and implementation to enhance downstream platforms and improve process efficiency.

  • Author and review technical documents, development reports, SOPs, manufacturing batch records, and CMC sections of regulatory submissions (IND, INDa, BLA).

  • Transfer downstream processes to manufacturing sites, CMOs, and partner sites, ensuring successful scale-up and implementation.

  • Represent Downstream Process Development on cross-functional teams and contribute to strategic initiatives.

  • Produce significant internal/external documents or publications supporting company goals.

Basic Qualifications

  • BS degree with at least 8 years of industry experience in biopharmaceutical industry with expertise in protein purification (chromatography, depth/membrane filtration, ultrafiltration/TFF) and antibody-drug conjugates.

  • MS degree with at least 6 years of industry experience in biopharmaceutical industry with expertise in protein purification (chromatography, depth/membrane filtration, ultrafiltration/TFF) and antibody-drug conjugates.

  • Familiarity with protein conjugation process chemistry and formulation.

  • Hands-on experience in protein purification, thorough understanding of chromatography, and familiarity with AKTA systems.

  • Extensive knowledge of impurity removal strategies and product variant control; strong chromatography and/or conjugation experience preferred.

  • Proven track record in scaling up, transferring, and supporting purification processes from bench to pilot/commercial scale in GMP environments.

  • Experience with statistical design of experiments, advanced data analysis, process validation, and Quality by Design concepts.

  • At least 3+ years of experience supervising technical staff with strong management and leadership skills.

  • Excellent organizational skills and ability to manage multiple projects in a fast-paced environment.

  • Strong communication skills (verbal and written) and ability to build relationships across teams and with external partners.

Preferred Qualifications:

  • PhD with at least 2 years of experience in biopharmaceutical industry with expertise in protein purification (chromatography, depth/membrane filtration, ultrafiltration/TFF) and antibody-drug conjugates.


The salary range for this position is:

Bay Area: $169,320.00 - $219,120.00.


 

Other US Locations: $153,935.00 - $199,210.00.


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.


For jobs in the United States:

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.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the  legal duty to furnish information; or (d) otherwise protected by law.
 

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Top Skills

Akta Systems
Bioconjugation
Chromatography
Protein Purification
Ultrafiltration
HQ

Gilead Sciences Foster City, California, USA Office

333 Lakeside Drive, Foster City, CA, United States, 94404

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