QC Chemist III
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 This role will be a lab-based role in quality control at La Verne, CA responsible for GMP release and stability testing for drug substance and drug product samples in the biologics laboratory
Key Responsibilities
- Perform quality control release and stability testing on drug substance and drug product for product quality assays including but not limited to compendial methods, SEC (Size exclusion chromatography), cIEF (capillary isoelectric focusing), CE-SDS (capillary electrophoresis sodium dodecyl sulfate), CEX (cation exchange) Contribute to the method validation and/or transfers Perform data review and data verification of laboratory data for early-stage, late-stage
- commercial biologic programs Essential Duties and Job Functions: Knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices (GLPs) Work with electronic laboratory systems such as LIMS, ELN, LES
- EMPOWER Troubleshoot instrumentation and test methods within QC jurisdiction, as required.
- Support Quality Control functions and lab management The applicant should be an effective communicator of ideas, project goals
- results to team members across cross-functional roles/departments Candidates should be self-motivated and organized Knowledge, Experience and Skills: Ability to learn and apply knowledge of GMP/GLP practices in a Laboratory Experience with High-Performance Liquid Chromatography (HPLC), ProteinSimple Maurice, and/or Beckman PA800 plus CE Able to write standard operating procedures (SOPs), test methods
- protocols Perform job functions with a quality mindset Working knowledge and proficiency with Microsoft Office software Work independently and in a team setting Demonstrate good verbal communication skills and interpersonal skills Be able to work in a fast-paced and highly collaborative working environment
Basic Qualifications
- BS degree in Microbiology, Chemistry, Biology, or equivalent scientific discipline with at least 4 years of relevant experience.
- OR MS degree in Microbiology, Chemistry, Biology, or equivalent scientific discipline with at least 2 years of relevant experience.
- Advanced knowledge of current GMP/GLP practices The salary range for this position is: $92,820.00 - $120,120.00.
- 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
- is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds
- 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
- 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
- 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.
- For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.
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- 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.
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- Our workforce reflects these values and celebrates the individuals who make up our growing team.
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- For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.