Senior Research Scientist II, Downstream Process Development, Oceanside CA


: $134,070.00 - $157,700.00 /year *

Employment Type

: Full-Time


: Scientific Research

Senior Research Scientist II, Downstream Process Development, Oceanside CA Job Description Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. By joining Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases. Gilead has an opportunity for an experienced candidate in our Biologics Development group at our Oceanside facility in Southern California. We are seeking motivated, team-oriented individuals with scientific expertise in Downstream Process Development as well as clinical and commercial operations related to recombinant proteins. Reporting to a Director, Downstream Development, Biologics, you will have the opportunity to work in teams for the early and late stage development of our protein molecules. Specific Responsibilities: Lead phase-appropriate downstream process development and technology transfer activities for monoclonal antibody, recombinant protein, and novel platform programs Set strategy for process scale-up, FMEAs, process robustness and characterization studies, process validation, and regulatory filings Review GMP and non-GMP technical documentation (batch records, SOPs, validation protocols & reports; process characterization protocols and reports) Support investigations and identify root causes for critical deviations Support internal and external manufacturing including travel to sites Participate on and lead cross-functional CMC teams Demonstrate hands-on technical leadership in the laboratory, oversee and delegate experimental/project responsibilities as needed, and write/review development summary reports and author sections of regulatory submissions. Be an effective communicator of ideas, project goals and results to team members across functional roles/departments. Proactively identify issues and develop solutions in a collaborative multidisciplinary environment. Be self-motivated and organized, familiar with the relevant literature, and enjoy scientific investigation and thinking. Lead, motivate, and develop the people in their group. Routinely make decisions affecting direction of project to ensure project timelines are met. Knowledge, Experience and Skills: PhD in a relevant scientific discipline with 7 years of industry experience. BS or MS degree with extensive industry experience. Supervisory experience is required. Experience from clinical process development to licensure and commercial manufacturing is preferred For jobs in the United States: As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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 for assistance. For more information about equal employment opportunity protections, please view the EEO is the Law poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT PAY TRANSPARENCY NONDISCRIMINATION PROVISION 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. To apply, visit:

Associated topics: aseptic, aseptic technique, biomedical, diet, dietary, immunoassay, immunohematology, medicine, nephrology, vaccine * The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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