Quality Document coordinator

We are seeking a detail-oriented and proactive Document Control & Compliance Specialist to support our quality systems within a GLP (Good Laboratory Practice) environment. This is a vital role where your expertise in documentation, training compliance, and regulatory processes will ensure the integrity and audit-readiness of our laboratory operations.

Qualifications:

Bachelor’s degree in Biology, Chemistry, or a related scientific field preferred.

Must 5+ years of experience in quality, documentation, or compliance within a GLP or cGMP setting.

Proven experience in document control, including formatting, tracking, and regulatory routing.

Experience with Veeva Quality Vault and Training Vault highly preferred.

Familiarity with GLP regulations (21 CFR Part 58) and R&D document workflows