Posted yesterday
Pharmaceutical Quality GLP Auditor (Consulting)
@ Consulting
Wawa, Ontario
Overview
Advarra is hiring Good Laboratory Practice (GLP) Auditors for its consultant network on Canada-based projects. The role plans and conducts GLP audits of CROs, central labs and vendors, then writes findings and root-cause reports. Candidates need 10+ years of QA or GLP experience, 5+ years of GLP auditing, and a bachelor's degree.
Responsibilities:
- Conduct GLP audits, including planning, agenda, audit and report writing
- Evaluate CRO, central lab and vendor compliance and qualification
- Prepare audit reports detailing findings and root causes
- Support corrective actions and present findings to QA leadership
Requirements summary:
- 10+ years of QA or GLP experience
- 5+ years of GLP auditing experience
- Experience with FDA and EMA expectations
- Bachelor's degree
- B2 level English, verbal and written
Source and dates
Employer career site / ATS feed · ultipro
- Employer posting date
- 2026-11-06
- First seen by our source
- 2026-11-06
- Source record updated
- 2026-11-06
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Senior |
| Department | Quality assurance |
| Experience | 10+ years |
| Hours per week | 40 (estimated) |
| Travel | air: moderate · ground: moderate |
| Work setting | Client sites, Office, Laboratory |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (required) |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Consulting
| Field | Value |
|---|---|
| Open jobs on Jobsy | 1 |
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Location
This role is open to candidates based in Canada.
Company Information
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.
Company Culture
Our people--both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
Job Overview Summary
Advarra is seeking Good Laboratory Practice (GLP) Auditors to join our consultant network for Canada-based projects. Auditors support compliance reviews across GLP sites and vendors.
Job Duties & Responsibilities
- Conduct Good Laboratory Practice (GLP) audits (planning, agenda, physical or remote audit, 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.
- If required will provide corrective actions support and present findings to QA leadership and stakeholders
- Work collaboratively with clients to ensure quality standards.
Basic Qualifications
- 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
Preferred Qualifications
- 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.
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