RPM ReSearch

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Quality Assurance Associate - 1637732 (KNA)

St. Kitts & Nevis

A Quality Assurance Associate supporting a GLP-compliant preclinical testing facility in St. Kitts: helping lead facility and study audits, reviewing protocols and SOPs, maintaining signed inspection records, and delivering GLP training. Core focus is lab QA compliance rather than software.

Gap Analysis Regulatory Compliance

Quality Assurance Specialist - 1637716 (KNA)

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A Quality Assurance Specialist at a GLP testing facility supports the QA Director by auditing studies, protocols, SOPs, and vendors to maintain Good Laboratory Practice compliance in preclinical drug development, including training staff and hosting regulatory audits. Requires a life-sciences degree and 5+ years of QA experience with 21 CFR Part 58.

NewBe an early applicant North America

Director QA/QC GLP In Vivo Operations (FL, USA)

Corrective Action Regulatory Compliance

Director-level QA/QC leader guiding an in vivo research organization (translational medicine/biotech) in Florida through its journey to FDA GLP compliance, including 21CFR Part 11. Day to day: building QA/QC strategies and SOPs, running audits, leading data integrity programs, training staff, and supporting compliant electronic systems. Requires bilingual English/Spanish.

NewBe an early applicant North AmericaContract

Director of Quality Assurance, GLP QAU (Solana Beach, CA)

Backbone.js Regulatory Compliance Root Cause Analysis

Director-level role building a GLP Quality Assurance Unit from scratch at a preclinical in vivo research facility in Solana Beach, CA. The hire sets up SOPs, audit programs, and CAPAs, ensures FDA/USDA/AAALAC and 21 CFR Part 11 compliance, leads inspections, and grows a QA team, starting with paper-based systems before moving to tools like Pristima or Provantis.

NewBe an early applicant North AmericaContract

GLP Quality Assurance Manager, Contract Research Organization (Scranton, PA)

Corrective Action Risk Assessment

Leads daily GLP quality assurance at a contract research organization in Scranton, PA: managing a small QA team, running nonclinical study, in-life, process, data, and facility audits against 21 CFR Part 58/Part 11 and SOPs, and serving as the onsite QA point of contact for client and regulatory audits.

NewBe an early applicant North AmericaContract

GLP Quality Assurance Specialist (San Diego, CA)