Quality Control Analyst II

The PositionA healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.In Pharma Technical Development, we actively collaborate and develop creative technical solutions to efficiently transform scientific ideas into products that reliably deliver our pipeline to patients. As a Lab Analyst, you will join our Global Analytical Development and Quality Control team, a leader in developing and executing testing methods for our biologics pipeline. You will contribute to our mission through innovation, teamwork, and continuous improvement in a dynamic environment.The OpportunityYou perform a broad variety of basic and complex physico-chemical tests for biologics and other pharmaceutical compounds according to GMP.You maintain accountability for deliverables affecting department goals and maintain a state of inspection readiness.You identify discrepancies and support the resolution of technical problems to assist the department in meeting corporate objectives.You schedule and execute routine and semi-routine assignments while supporting general lab maintenance operations.You ensure the integration of environmental health, safety, and security into business processes, reporting any safety and environmental incidents within your functional area.You adhere to cGMP policies and procedures, ensuring accurate documentation of activities and transactions in applicable systems.You coordinate with customers to support operational activities and actively participate in group and project teamwork.Who you areYou possess a Bachelor's degree, preferably in a scientific discipline, 2 to 4 years of related experience in a lab environment.You communicate clearly and effectively, both verbally and in writing.You exercise sound judgment, reasoning, and problem-solving capabilities.You demonstrate attention to detail with strong organization and prioritization skills.You take accountability and work effectively as part of a collaborative team.Preferred:You preferably have previous GMP experience in a biopharmaceutical environment.You possess QC / cGMP experience working in a lab environment in an industry or academic setting.Relocation benefits are not available for this posting.The expected salary range for this position based on the primary location of South San Francisco, CA is 78 500,00 - 145 900,00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.BenefitsGenentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202608-122155Date posted : 2026-09-08Profession: Regulatory & QualityEmployment type: Full time