QA Program Lead - Quality Systems & Documentation
Rigel Pharmaceuticals
Rigel Pharmaceuticals Inc. in South San Francisco is seeking a Quality Assurance Program Manager to provide operational support for the Quality Assurance organization. This role coordinates critical QA activities across multiple priorities, ensuring compliance with GxP operations and delivering high-quality work. The ideal candidate will have a Bachelor's degree, at least six years of relevant experience, and strong skills in Quality Systems and Document Control. A comprehensive benefits package is offered. #J-18808-Ljbffr Rigel Pharmaceuticals
$140k - $170k
Position Summary The Quality Assurance Program Manager is responsible for providing operational support... ...role coordinates business‑critical QA activities across multiple concurrent priorities while managing Quality Systems, Document Control, and Learning Management...QualityFlexible hours$112k - $140k
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...full-time development program to transition into accredited... ...against ISO management system standards, primarily... ...ISO requirements Document audit findings clearly... ...science, environmental, quality, industrial, or a related... ...or ISO 13485 Completed Lead Auditor training for ISO...QualityPermanent employmentFull timeContract workFreelanceLocal area$150k - $170k
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