Pharmaceutical Quality GLP Auditor – Consulting

Advarra

. Conduct Good Laboratory Practice (GLP) audits, including planning, agenda preparation, physical or remote audits, and report writing .

Posted 11/7/2026full-timeRemote • CanadaSeniorLeadWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Expertise in conducting Good Laboratory Practice (GLP) audits and developing quality assurance plans, with a strong focus on regulatory compliance and stakeholder communication. Proven ability to prepare detailed audit reports and provide corrective action support in a collaborative environment.

Highest-signal resume keywords

Good Laboratory Practice (GLP) AuditingQuality Assurance ExperienceRegulatory Compliance (FDA, EMA)Audit Report WritingB2 Level English Communication

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Good Laboratory Practice (GLP)Quality Assurance PlansAudit ProgramsCorrective Action PlansRegulatory Agency ExpectationsAudit Readiness ActivitiesAnalytical SkillsProblem-Solving SkillsReport Writing

Soft Skills

Interpersonal SkillsClient Interaction SkillsCommunication SkillsCollaboration Skills

Industry Keywords

CRO EvaluationCentral Labs ComplianceVendor QualificationStakeholder InteractionAdvarra Consultant Network

About the role

Key responsibilities & impact

Conduct Good Laboratory Practice (GLP) audits, including planning, agenda preparation, physical or remote audits, and report writing
Evaluate CROs, Central Labs, and vendor compliance or qualification
Prepare comprehensive audit reports detailing findings and root causes
Provide written audit reports in English
Provide corrective action support and present findings to QA leadership and stakeholders when required
Work collaboratively with clients to ensure quality standards
Join Advarra’s consultant network for Canada-based projects

Requirements

What you’ll need

Minimum 10+ years of Quality Assurance and/or Good Laboratory Practice (GLP) experience
Minimum 5+ years of Good Laboratory Practice (GLP) auditing experience
Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities
Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans
B2 level in English communication, verbal and written
Bachelor's degree
Strong interpersonal and client interaction skills
Excellent analytical, problem-solving, communication, and report-writing skills
Ability to work collaboratively across departments and interact with internal and external stakeholders
Candidates must be based in Canada
Registration using the Expert Enrollment Form is required for candidates not already part of the Advarra network

Benefits

Comp & perks

Inclusive and collaborative work environment
Consultant network opportunities
Opportunity to support clinical research and advance patient health
Reasonable accommodation available for applicants with disabilities