Senior Associate Scientist — Quality Control Biologics

2 weeks ago


Foster City, United States Gilead Sciences, Inc. Full time

Senior Associate Scientist — Quality Control Biologics (Clinical Analytical Operations) Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life‑threatening diseases, including HIV, viral hepatitis, and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California. Key Responsibilities Clinical Analytical Operations: The role is vital for the success of Clinical Biologics QC, providing support for strategic leadership and oversight of daily operations. Manage release testing supporting Gilead’s Clinical biologics drug substances and drug products. Contribute to refining QC procedures across Gilead’s biologics manufacturing network, ensuring compliance with global cGMP and Gilead’s Quality Management System. Job Responsibilities Experience with Biologics Quality Control sub‑functions and extensive knowledge of industry best practices and trends. Experience or demonstrated capacity to learn GMP principles, concepts, practices and standards in the US and internationally. Develop and improve complex concepts, techniques, and standards and new applications based on quality principles and theories. Develop solutions to complex problems, requiring a high degree of ingenuity, creativity and innovativeness. Exercise judgment and independently determine and take appropriate action where precedent may not exist. Work with senior management to develop and ensure support for company‑wide long‑term solutions. Manage and influence Quality Control testing at contract laboratory facilities and ensure alignment with Gilead’s GMP policies. Influence process and outcomes across functions. Support future laboratory work. Support Commercial QC team. Basic Qualifications Master’s Degree in Chemistry, Biochemistry or related field and 3+ years of relevant experience Bachelor’s Degree in Chemistry, Biochemistry or related field and 5+ years of relevant experience Associate’s Degree in Chemistry, Biochemistry or related field and 7+ years of relevant experience High School Degree and 9+ years of relevant experience Preferred Qualifications Experience in a lab environment, including knowledge of analytical testing, familiarity with laboratory instrumentation. Experience with GMP systems such as LIMS, QMS, SAP. Experience with software such as JMP, Discoverant, Empower. Experience in biopharmaceutical or pharmaceutical quality control. Stays ahead of shifting trends in industry. Strong critical and creative thinking, able to work independently to determine appropriate resources for resolution of problems. Strong organizational and planning skills. Excellent verbal and written communication skills and collaborative interpersonal skills. Job Requisition ID R Full Time/Part Time: Full‑TimeJob Level: AssociateRemote Type: Onsite Required #J-18808-Ljbffr



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