Gilead Sciences-posted 12 days ago
Full-time • Mid Level
Foster City, CA
5,001-10,000 employees

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 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: Commercial Analytical Lifecycle Management: The Scientist, Analytical Lifecycle Management is vital for the success of C ommer cial Biologics QC, providing support for strategic leadership and oversight of daily operations. Responsibilities include supporting Commercial specification strategies, reference standard s , raw materials, and critical reagents programs, analytical method validations and transfers, and the compendial review program. The role will contribute to monitoring QC test method execution and leading the analytical lifecycle management of C ommercial biologics drug substances and drug products.

  • supporting Commercial specification strategies
  • reference standard s , raw materials, and critical reagents programs
  • analytical method validations and transfers
  • the compendial review program
  • monitoring QC test method execution
  • leading the analytical lifecycle management of C ommercial biologics drug substances and drug products
  • Experience over a broad set of Quality Control sub-functions with extensive knowledge of industry best practices and trends.
  • In-depth understanding and application of GMP principles, concepts, practices and standards in the US and internationally.
  • Must be able to develop and improve complex concepts, techniques, and standards and new applications based on quality principles and theories.
  • Must be able to develop solutions to complex problems, which require a high degree of ingenuity, creativity and innovativeness.
  • Must be able to exercise judgment and independently determine and take appropriate action where precedent may not exist.
  • Proven ability to work with senior management to develop and ensure the implementation of Company-wide long-term solutions.
  • Demonstrated the ability to motivate and engage individuals.
  • Demonstrated the ability to influence process and outcomes across functions.
  • Willing to support future laboratory work.
  • Willing to support Commercial QC team.
  • PhD in Chemistry, Biochemistry or related field OR Master's Degree in Chemistry , Biochemistry or related field and 4+ years of relevant experience OR Bachelor's Degree in Chemistry , Biochemistry or related field and 6+ years of relevant experience OR Associate’s Degree in Chemistry , Biochemistry or related field and 8+ years of relevant experience OR High School Degree and 10+ years of relevant experience
  • Experience developing and/or leading reference standard and critical reagent programs for commercial or late-stage biologics drug substances and drug products products .
  • Experience authoring validation protocols and reports for commercial or late-stage products.
  • Experience leading or participating in the development of product specification setting for commercial or late-stage products.
  • 1+ year of relevant QC experience in a GMP Lab environment, including knowledge of analytical testing, familiarity with laboratory instrumentation and GMP systems/software ( e.g. LIMS, QMS, Empower) for biologics drug substances and drug products.
  • Experience in Biopharmaceutical or Pharmaceutical quality control.
  • Stays ahead of shifting trends in industry.
  • Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.
  • Strong organizational and planning skills .
  • Shows excellent verbal and written communication skills and collaborative interpersonal skills.
  • 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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