Assoc Director, Quality Assurance GMP
Erasca · South San Francisco, CA; San Diego, CA; remote
Posted 28 days ago · $175,000 to $210,000
or apply directly on Erasca's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 28 days Erasca's roles stay open a median of 43 days
- Reposted
- No
- Salary listed
- Yes 100% of Erasca's roles list one
- Ghost-job risk at Erasca
- high 5 stale, 0 reposted of 10 open
- Hiring momentum
- 13 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Erasca's own greenhouse board since 2026-08-03. Full hiring picture for Erasca.
About this role
The Associate Director of Quality Assurance GMP at Erasca will oversee GMP clinical manufacturing operations, ensuring compliance with quality standards and regulations. Responsibilities include reviewing and approving batch records, managing quality events, and liaising with internal and external stakeholders. The role also involves vendor management, compliance audits, and supporting the quality management system.
- benefits
- 5/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Erasca as an employer.
What you need
- Bachelor of Science in Biology, Chemistry, Physical Sciences, or related degree
- 8+ years of progressive industry experience in pharmaceutical small molecule drug product development
- 8-10 years in GxP pharmaceutical environment in progressively responsible Quality roles
- Minimum of 8 years of GMP QA experience
- Previous Quality oversight/support experience in solid oral dosage and Biologics manufacturing
- Strong interpersonal, verbal, and written communication skills
Nice to have
- Advanced degree in Pharmaceutics, Chemistry or related field
- Quality Systems experience
- Experience with electronic document management systems and Quality Management System software platforms
- Previous experience working with FDA and participating in regulatory agency inspections
- Previous experience working with non-US regulatory agencies and/or international product supply
What you get
- Paid Time Off, Holiday, and Sick Leave
- Medical, Dental and Vision Plans
- Short- and Long-Term Disability
- Basic and Voluntary Life/AD&D Coverage
- Flexible Spending Accounts (FSA, HSA, and Commute)
- Critical Illness and Accident Coverage
Worth weighing
- Salary range provided is broad and dependent on various factors
- Role involves significant oversight responsibilities which may lead to high pressure
- Experience with international product supply and regulatory agencies is preferred but not mandatory
Summarised from Erasca's posting. Read the full original.
Listed by Erasca on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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