Principal Quality/GxP Auditor - 4984

Posted 8 Days Ago
Be an Early Applicant
Las Vegas, NV
85K-173K Annually
7+ Years Experience
Pharmaceutical
The Role
The Principal Quality/GxP Auditor is responsible for developing compliance plans, providing mentorship, supporting audits, and ensuring client compliance with industry regulations. This role requires expert knowledge of GxP regulatory requirements and FDA laws, along with the ability to deliver industry lectures and training.
Summary Generated by Built In

Top Skills

Microsoft Project
The Company
HQ: Fishers, IN
402 Employees
On-site Workplace
Year Founded: 2020

What We Do

Verista is a leading business and technology consultancy firm that provides systems, compliance, validation and quality solutions to life science companies - enabling them to improve health and improve lives. We help clients solve their most critical and complex challenges across the GxP lifecycle, from preclinical and clinical to commercialization, manufacturing and distribution – bringing together decades of knowledge, the most advanced engagement platforms and transformative technologies. This allows clients to benefit from the ease, efficiency and trust that results from working with one partner who excels across specialties. Verista’s clients trust the company’s 650+ experts to deliver consistent, safe, and high-quality results across the product development lifecycle. Verista is based in Fishers, Indiana, Wayne, Pennsylvania, Westford, Massachusetts, and San Mateo, California. For more information, visit www.verista.com

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