Senior Quality Assurance Auditor

Job Category
:
Quality Assurance and Compliance

Requisition Number
: SENIO
002809

• Posted :
  October 2, 2026
• Full-Time

Showing 1 location

Remote
Canada

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s Corporate headquarters are located in Ontario, Canada and US headquarters in New Jersey, USA, with additional physical offices in Asia and Europe.

Everest is known in the industry for its high-quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.

To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior QA Auditor
for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.

RESPONSIBILITIES INCLUDE:

Complete scheduled internal audits to assess compliance with applicable regulatory requirements and Everest Standard Operating Procedures (SOPs).

Document and report audit findings in a timely manner.

Lead corrective and preventative actions investigations and follow-up on compliance issues until resolution.

Maintain the company’s governing documents according to SOPs including, but not limited to, entering the governing document tracking information into a database, updating database records when governing documents are updated, and reporting and following-up on outstanding SOP review obligations.

Assist with external audits by clients and regulatory inspections.

Independently conduct vendor qualification assessments. Coordinate the assessment effort and follow up on observations as needed.

Conduct employee training of QA procedures.

Follow up with Project Managers or Project Oversight personnel to ensure that study-specific training, Project Kick-off Meeting (including study-specific training components), or training of Sponsor specific requirements (such as Sponsor-specific serious adverse event handling procedures, etc.) are properly conducted by project teams.

Follow up on industry best working practices in quality control (QC) and QA by researching and participating in relevant training and/or association activities.

REQUIREMENTS:

Bachelor’s degree in health science, physics, biology, or mathematics.

Certification as a quality auditor from the American Society of Quality (ASQ), ISO, or equivalent is preferred.

At least 6 years of QA experience in a clinical research capacity. Significant contribution, outstanding and sustained performance in a non-QA role may be used in lieu of the requirement on the number of years of relevant QA experience.

At least 1 year experience with participation in preparations/hosting regulatory inspections is preferred.

Knowledge of clinical trial processes and procedures.

Knowledge of pharmaceutical industry regulatory requirements for differing governing bodies such as FDA, Health Canada, European Medicines Agency,…