Associate Quality Lead
$89,100–$165,500 year
On-site · South San Francisco, California, United States
Job Summary
Associate Quality Lead in Pharma Development Quality (PDQ) leading risk-based quality strategies, delivering QA activities, managing quality data, and presenting to Health Authorities. Collaborates across functions to ensure regulatory data integrity, supports GxP inspections (scribe duties and document QC), champions adoption of digital tools, and drives process mapping within QMS. Onsite role based in South San Francisco, leveraging data analytics to deliver high-quality insights and foster continuous improvement in patient outcomes.
Required Qualifications
- Bachelor’s degree in a scientific or quality-related discipline, or an equivalent combination of education and experience
- Experience within the pharmaceutical, biotech, or medical device industry, with understanding of GxP regulations (GCP, GVP, MDR)
- Strong digital and data literacy with ability to interpret data into actionable quality insights
- Exceptional organizational and execution skills, ownership of projects
- Developing expertise in CtQ factors and functional group operations
- Fluency in written and spoken English with strong presentation skills
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