GCP Quality Assurance Director

HIRING: Associate Director or Director, GCP Quality Assurance - Growing Oncology Biotech - Maryland
Hays Life Sciences is currently partnered with a rapidly growing oncology biotechnology company to assist them in their search for a remote-based GCP Quality Assurance Director. This company boasts an impressive portfolio of drug candidates targeted for various oncology indications. As they progress through clinical development, they are looking to fast-track their headcount growth. The GCP Quality Assurance Director will work in a highly visible capacity and as such, there is excellent career growth potential in this role.

In this capacity, you will be responsible for leading and providing the strategic Quality vision for the company’s clinical development efforts. You will develop quality risk mitigation strategies, perform risk assessments, conduct internal and vendor audits, develop and maintain audit tools and author and review audit reports. In addition, you will communicate critical audit findings and significant deviations to executive management.

At minimum, you must possess a Bachelor’s degree in a scientific discipline, 5+ years of direct GCP QA experience in the pharmaceutical or biotechnology industry, 3+ years of clinical trial monitoring and/or pharmacovigilance experience, and experience leading internal and external quality audits. Experience with FDA inspections is required.

Apply now for consideration.


Job type:
Full Time
Competitive / Based on Experience
Apply Now

Talk to a consultant

Talk to Phu Huynh, the specialist consultant managing this position, located in New York City

16th Floor, 200 West 41st St

Telephone: 212 548 4525

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