CQV Associate Director

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WHEN YOU NEED TO MEET A HIGHER STANDARD® in US | ASIA | EUROPE | AUSTRALIA

CQV • Start-Up and Verification • Owner's Project Management • Continuous Improvement • Asset Management

501 - 1000

Description

• The CQV Associate Director is a recognized CQV subject matter expert • Can act in a project oversight role, managing client relationships for multiple sites simultaneously • Engages in strategic project work to deliver special expertise • Supports the client project teams • Provides consulting to clients in best-in-class CQV methods

Requirements

• BS or MS in a relevant science or engineering field, or equivalent • Seven (7) or more years in CQV SME or project manager for large CQV projects roles for life sciences • Excellent oral and written communication skills in English • Excellent skill in leading teams to perform complex tasks under pressure • Excellent problem-solving skills • Customer-service focused • Proficient in life science manufacturing processes in areas such as biotech, aseptic fill/finish, OSD, Gene Therapy or equivalent experience • Able to travel domestically and internationally if required

Benefits

• up to 15% retirement contribution • 24 days PTO and 5 sick days per year • health insurance at extremely low cost to employee • financial support for both internal and external professional education • 70% long term disability paid for by the company