Gilead Sciences, Inc.
Sr Research Associate, Process Development
Gilead Sciences, Inc., Oceanside, California, United States, 92058
Sr Research Associate, Process Development
United States - California - Oceanside Process/Product Development & Operations Regular
Job Description 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.
The Senior Research Associate in the Biologics Pivotal & Commercial Cell Culture Process Development function will execute cell culture process development laboratory experiments for Gilead biologics entities during pivotal development (phases II/III, commercial). They will also support cell culture process technology development, platform process initiatives, and implementation of cell culture processes in pilot plant and GMP facilities. At a future date this position will relocate to the corporate HQ in Foster City, CA.
Key Responsibilities
Plan and execute experiments to support cell culture process optimization and characterization during pivotal development phases.
Support cell culture platform development and pilot plant operations, as needed.
Maintain a state-of-the-art cell culture process development laboratory, including equipment upkeep and consumables management.
Participate in equipment maintenance and continued improvement of lab and data handling best practices.
Ensure high-quality and timely documentation of data in electronic laboratory notebooks.
Collect, analyze, and visualize data from laboratory experiments.
Present results of work, interpret data, and draw conclusions regarding presented material and nature of work.
Author experimental protocols and reports.
Travel as required to support technology transfers and provide oversight at both internal and external manufacturing facilities.
Adhere to department budget and all trainings, regulatory compliance, and safety requirements.
Basic Qualifications
Degree in a relevant scientific discipline (e.g., bioengineering, chemical engineering, biochemical engineering).
Bachelor's degree and 2+ years of relevant experience; OR
Master's degree and 0+ years of relevant experience.
Preferred Qualifications
Hands‑on laboratory operations experience including shake flasks, high‑throughput bioreactors, bench‑scale bioreactors, and pilot‑scale bioreactors.
Experience in pivotal stage cell culture process development and implementation in GMP facilities.
Excellent communication, technical writing, presentation skills and aptitude for creative problem solving.
Demonstrated ability to collaborate, work in a team setting, and influence cross‑functionally.
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.
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 ApplicantAccommodations@gilead.com for assistance.
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.
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Job Description 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.
The Senior Research Associate in the Biologics Pivotal & Commercial Cell Culture Process Development function will execute cell culture process development laboratory experiments for Gilead biologics entities during pivotal development (phases II/III, commercial). They will also support cell culture process technology development, platform process initiatives, and implementation of cell culture processes in pilot plant and GMP facilities. At a future date this position will relocate to the corporate HQ in Foster City, CA.
Key Responsibilities
Plan and execute experiments to support cell culture process optimization and characterization during pivotal development phases.
Support cell culture platform development and pilot plant operations, as needed.
Maintain a state-of-the-art cell culture process development laboratory, including equipment upkeep and consumables management.
Participate in equipment maintenance and continued improvement of lab and data handling best practices.
Ensure high-quality and timely documentation of data in electronic laboratory notebooks.
Collect, analyze, and visualize data from laboratory experiments.
Present results of work, interpret data, and draw conclusions regarding presented material and nature of work.
Author experimental protocols and reports.
Travel as required to support technology transfers and provide oversight at both internal and external manufacturing facilities.
Adhere to department budget and all trainings, regulatory compliance, and safety requirements.
Basic Qualifications
Degree in a relevant scientific discipline (e.g., bioengineering, chemical engineering, biochemical engineering).
Bachelor's degree and 2+ years of relevant experience; OR
Master's degree and 0+ years of relevant experience.
Preferred Qualifications
Hands‑on laboratory operations experience including shake flasks, high‑throughput bioreactors, bench‑scale bioreactors, and pilot‑scale bioreactors.
Experience in pivotal stage cell culture process development and implementation in GMP facilities.
Excellent communication, technical writing, presentation skills and aptitude for creative problem solving.
Demonstrated ability to collaborate, work in a team setting, and influence cross‑functionally.
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.
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 ApplicantAccommodations@gilead.com for assistance.
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.
#J-18808-Ljbffr