Lab Compliance Manager
Vaxcyte · San Carlos, California, United States
Posted 20 days ago · $153,000 - $178,000
or apply directly on Vaxcyte's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 20 days Vaxcyte's roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- Yes 90% of Vaxcyte's roles list one
- Ghost-job risk at Vaxcyte
- high 39 stale, 0 reposted of 49 open
- Hiring momentum
- 71 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 Vaxcyte's own greenhouse board since 2026-08-03. Full hiring picture for Vaxcyte.
About this role
The Lab Compliance Manager at Vaxcyte will oversee compliance within the Analytical Development laboratories, ensuring adherence to GMP standards as the labs transition to a GMP-compliant environment. This role involves managing the Sample Management Specialist, authoring laboratory-specific SOPs, and implementing quality processes in collaboration with Quality Assurance. The manager will also maintain inspection readiness and support training for laboratory personnel.
- benefits
- 2/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- 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 Vaxcyte as an employer.
What you need
- Bachelor's degree in a life sciences discipline or equivalent experience
- 8+ years of experience in a compliance, quality, analytical, or laboratory role within the biopharmaceutical or vaccine industry
- Working knowledge of GMP and/or GLP principles
- Experience authoring or contributing to controlled documents in a regulated environment
- Familiarity with data integrity principles (ALCOA+) and Good Documentation Practices (GDP)
- Experience executing or supporting equipment qualification activities in a regulated laboratory
Nice to have
- Experience at a clinical-stage biopharmaceutical or vaccine company
- Familiarity with FDA expectations for Phase I/II QC or analytical laboratory operations
- Experience with electronic laboratory or quality systems such as Benchling or LIMS
- Exposure to 21 CFR Part 11 compliance
- Prior experience supporting internal audits or regulatory inspections
What you get
- Competitive compensation package
- Comprehensive benefits
- Equity component
Worth weighing
- Hybrid work arrangement requires a minimum of 3 days per week onsite
- No specific salary details provided beyond the range
- Role involves significant compliance responsibilities which may be challenging in a transitioning environment
Summarised from Vaxcyte's posting. Read the full original.
Listed by Vaxcyte on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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