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Key Responsibilities:
- Provide QA oversight for GMP manufacturing, product release, and analytical data review for biologic and small molecule products.
- Manage quality agreements, vendor audits, and support regulatory inspections.
- Author and review SOPs, policies, and quality system documents.
Qualifications:
- Bachelor's in Biology or related field; advanced degree preferred with 8+ years in pharmaceutical GxP roles.
- Minimum 8 years of GMP QA experience, including solid oral dosage and biologics manufacturing.
- Experience with FDA and international regulatory agencies.
Compensation and Benefits:
- Competitive base salary range of $175,000 - $210,000 plus annual bonus and equity.
- Comprehensive benefits including medical, dental, vision, 401(k) with company contribution, and employee stock purchase program.
- Generous paid time off, holidays, and sick leave in a collaborative and mission-focused environment.
Erasca
Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for patients with cancer, targeting the RAS/MAPK pathway. With a small, collaborative team and a casual, mission-driven culture, they are committed to erasing cancer.